V CFH | |||
This variant could not be mapped to the genome. Associations 2 Studies 2 |
G CFH | |||
Description: complement factor H Associations 1964 Studies 1871 |
P CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy. | |||
Hosoda Y et al. 2018 Proc Natl Acad Sci U S A PMID:29844195 Associations 2 Studies 1 |
P Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. | |||
McCormack M et al. 2017 Neurology PMID:29288229 Associations 2 Studies 4 |
P Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. | |||
Davila S et al. 2010 Nat Genet PMID:20694013 Associations 1 Studies 1 |
P Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis. | |||
de Groot EL et al. 2023 JAMA Ophthalmol PMID:37410486 Associations 1 Studies 1 |
P Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration. | |||
Lorés-Motta L et al. 2018 Ophthalmology PMID:29398083 Associations 2 Studies 1 |
P Citrullinated and MMP-degraded vimentin is associated with chronic pulmonary diseases and genetic variants in PADI3/PADI4 and CFH in postmenopausal women. | |||
Bager CL et al. 2023 Sci Rep PMID:38155185 Associations 11 Studies 1 |
P Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. | |||
Lorés-Motta L et al. 2021 Am J Hum Genet PMID:34260947 Associations 12 Studies 6 |
V rs1061147 | |||
Location: 1:196685194 Cytogenetic region:1q31.3 Most severe consequence: Synonymous variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs1061170 | |||
Location: 1:196690107 Cytogenetic region:1q31.3 Most severe consequence: Missense variant Mapped gene(s): CFH Associations 8 Studies 8 |
V rs1329424 | |||
Location: 1:196677046 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 93 Studies 93 |
V rs380390 | |||
Location: 1:196731921 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10801555 | |||
Location: 1:196691131 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 88 Studies 88 |
V rs1410996 | |||
Location: 1:196727803 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 7 Studies 7 |
V rs3753394 | |||
Location: 1:196651787 Cytogenetic region:1q31.3 Most severe consequence: Regulatory region variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs800292 | |||
Location: 1:196673103 Cytogenetic region:1q31.3 Most severe consequence: Missense variant Mapped gene(s): CFH Associations 7 Studies 7 |
V rs6677604 | |||
Location: 1:196717788 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 9 Studies 7 |
V rs1329428 | |||
Location: 1:196733680 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 11 Studies 11 |
V rs1831282 | |||
Location: 1:196704863 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs10737680 | |||
Location: 1:196710325 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 10 Studies 10 |
V rs10801558 | |||
Location: 1:196729914 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs10922108 | |||
Location: 1:196732343 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs10922106 | |||
Location: 1:196722334 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs6677089 | |||
Location: 1:196715183 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs10922105 | |||
Location: 1:196721120 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922104 | |||
Location: 1:196718600 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs3753395 | |||
Location: 1:196717522 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs10465586 | |||
Location: 1:196718199 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs2274700 | |||
Location: 1:196713817 Cytogenetic region:1q31.3 Most severe consequence: Synonymous variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs7535263 | |||
Location: 1:196713216 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs1329427 | |||
Location: 1:196735429 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs7540032 | |||
Location: 1:196732154 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10801559 | |||
Location: 1:196735074 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs7514261 | |||
Location: 1:196731784 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs6688272 | |||
Location: 1:196715262 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs3766405 | |||
Location: 1:196726031 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs10922109 | |||
Location: 1:196735502 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs570618 | |||
Location: 1:196687934 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 11 Studies 11 |
V rs121913059 | |||
Location: 1:196747245 Cytogenetic region:1q31.3 Most severe consequence: Missense variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs35292876 | |||
Location: 1:196737512 Cytogenetic region:1q31.3 Most severe consequence: Synonymous variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs35908703 | |||
Location: 1:196723810 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs419137 | |||
Location: 1:196727745 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs6695321 | |||
Location: 1:196706731 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 18 Studies 18 |
V rs7529589 | |||
Location: 1:196689149 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 7 Studies 7 |
V rs1048663 | |||
Location: 1:196705852 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10733086 | |||
Location: 1:196707805 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs3753396 | |||
Location: 1:196726612 Cytogenetic region:1q31.3 Most severe consequence: Missense variant Mapped gene(s): CFH Associations 4 Studies 3 |
V rs528298 | |||
Location: 1:196691865 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 104 Studies 104 |
V rs34813609 | |||
Location: 1:196699231 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 303 Studies 302 |
V rs368465 | |||
Location: 1:196702851 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs33944729 | |||
Location: 1:196682995 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 74 Studies 74 |
V rs140142103 | |||
Location: 1:196692601 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 5 Studies 5 |
V rs10754199 | |||
Location: 1:196701709 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 82 Studies 82 |
V rs12038333 | |||
Location: 1:196703324 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs7539005 | |||
Location: 1:196698122 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 12 Studies 12 |
V rs10801553 | |||
Location: 1:196686613 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 9 Studies 9 |
V rs529541 | |||
Location: 1:196750586 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 5 Studies 5 |
V rs28664709 | |||
Location: 1:196702087 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs11390840 | |||
Location: 1:196662875 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs70621 | |||
Location: 1:196735879 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 12 Studies 2 |
V rs70620 | |||
Location: 1:196735867 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs10801556 | |||
Location: 1:196691334 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs10801561 | |||
Location: 1:196745540 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs4658046 | |||
Location: 1:196701627 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 86 Studies 85 |
V rs35617250 | |||
Location: 1:196710552 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs6689009 | |||
Location: 1:196729333 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs34331968 | |||
Location: 1:196690623 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 9 Studies 9 |
V rs203688 | |||
Location: 1:196703255 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 31 Studies 31 |
V rs549213437 | |||
Location: 1:196658408 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs12134598 | |||
Location: 1:196711871 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs2019727 | |||
Location: 1:196705584 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs150313019 | |||
Location: 1:196750687 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs488380 | |||
Location: 1:196695375 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 6 Studies 6 |
V rs559350 | |||
Location: 1:196673403 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs114645367 | |||
Location: 1:196747868 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs12032372 | |||
Location: 1:196694724 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs572515 | |||
Location: 1:196677131 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 18 Studies 18 |
V rs6660100 | |||
Location: 1:196666552 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs551397 | |||
Location: 1:196672942 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922107 | |||
Location: 1:196729521 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs36137052 | |||
Location: 1:196697883 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs10922098 | |||
Location: 1:196695521 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 182 Studies 182 |
V rs16840522 | |||
Location: 1:196741786 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs529899 | |||
Location: 1:196698298 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs1065489 | |||
Location: 1:196740644 Cytogenetic region:1q31.3 Most severe consequence: Missense variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922092 | |||
Location: 1:196688284 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs12405238 | |||
Location: 1:196692483 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs140237249 | |||
Location: 1:196750545 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs529825 | |||
Location: 1:196665976 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs2300429 | |||
Location: 1:196706226 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922094 | |||
Location: 1:196692375 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs189711360 | |||
Location: 1:196721049 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs6677460 | |||
Location: 1:196715445 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs79190861 | |||
Location: 1:196730276 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs35352142 | |||
Location: 1:196743772 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922100 | |||
Location: 1:196696078 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 38 Studies 38 |
V rs113439691 | |||
Location: 1:196662986 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs12144939 | |||
Location: 1:196729815 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs28688002 | |||
Location: 1:196665337 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs402056 | |||
Location: 1:196702856 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 10 Studies 10 |
V rs10922102 | |||
Location: 1:196699157 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 5 Studies 5 |
V rs10801557 | |||
Location: 1:196700451 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 16 Studies 16 |
V rs506317 | |||
Location: 1:196748023 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs12038674 | |||
Location: 1:196696521 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs514591 | |||
Location: 1:196671190 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs200480894 | |||
Location: 1:196682520 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs1089033 | |||
Location: 1:196697663 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 17 Studies 17 |
V rs10922103 | |||
Location: 1:196701988 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 45 Studies 45 |
V rs12045503 | |||
Location: 1:196703343 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 51 Studies 51 |
V rs76258507 | |||
Location: 1:196696914 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 75 Studies 75 |
V rs61229706 | |||
Location: 1:196692709 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 118 Studies 118 |
V rs1329421 | |||
Location: 1:196687075 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 21 Studies 21 |
V rs12033127 | |||
Location: 1:196695125 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 49 Studies 49 |
V rs1329422 | |||
Location: 1:196686150 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 13 Studies 13 |
V rs10922097 | |||
Location: 1:196695352 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 10 Studies 10 |
V rs374896 | |||
Location: 1:196723248 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs3645 | |||
Location: 1:196693886 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs10922096 | |||
Location: 1:196693329 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs12029785 | |||
Location: 1:196689775 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs9970075 | |||
Location: 1:196704300 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs731557 | |||
Location: 1:196735885 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10801554 | |||
Location: 1:196688525 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs2860102 | |||
Location: 1:196699189 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 5 Studies 5 |
V rs5016801 | |||
Location: 1:196665380 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 5 Studies 5 |
V rs12759472 | |||
Location: 1:196750817 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs2300430 | |||
Location: 1:196686583 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs482934 | |||
Location: 1:196689367 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs10922099 | |||
Location: 1:196695911 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs6664877 | |||
Location: 1:196715444 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs72734328 | |||
Location: 1:196698814 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs395544 | |||
Location: 1:196729142 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs579745 | |||
Location: 1:196695446 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 4 Studies 4 |
V rs12127759 | |||
Location: 1:196679483 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 3 Studies 3 |
V rs34388368 | |||
Location: 1:196666340 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs203676 (rs146862558) | |||
Location: 1:196714701 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs148553336 | |||
Location: 1:196644043 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs4657825 | |||
Location: 1:196615191 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 2 Studies 2 |
V rs58335053 (rs201263987) | |||
Location: 1:196702537 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 83 Studies 83 |
V rs1092801 | |||
Location: 1:196759905 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH,CFHR3 Associations 2 Studies 2 |
V rs481595 | |||
Location: 1:196647779 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs505102 | |||
Location: 1:196650372 Cytogenetic region:1q31.3 Most severe consequence: Regulatory region variant Mapped gene(s): CFH,KCNT2 Associations 2 Studies 2 |
V rs12061508 | |||
Location: 1:196615338 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 2 Studies 2 |
V rs10801551 | |||
Location: 1:196610909 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 2 Studies 2 |
V rs12029571 | |||
Location: 1:196634172 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 3 Studies 3 |
V rs77460977 | |||
Location: 1:196623549 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs371960809 | |||
Location: 1:196752801 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH,CFHR3 Associations 1 Studies 1 |
V rs3043084 | |||
Location: 1:196631261 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 3 Studies 3 |
V rs114489904 | |||
Location: 1:196643854 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs34845806 (rs559637118) | |||
Location: 1:196710780 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs47219 | |||
Location: 1:196629197 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 2 Studies 2 |
V rs11398897 (rs542832508) | |||
Location: 1:196708614 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 2 Studies 2 |
V rs200429765 (rs531067873) | |||
Location: 1:196679138 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH Associations 1 Studies 1 |
V rs139784897 | |||
Location: 1:196612631 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs17573358 | |||
Location: 1:196622341 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs443134 | |||
Location: 1:196758073 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH,CFHR3 Associations 1 Studies 1 |
V rs112916466 | |||
Location: 1:196620703 Cytogenetic region:1q31.3 Most severe consequence: Intergenic variant Mapped gene(s): CFH,KCNT2 Associations 1 Studies 1 |
V rs71131723 (rs138396963) | |||
Location: 1:196755855 Cytogenetic region:1q31.3 Most severe consequence: Intron variant Mapped gene(s): CFH,CFHR3 Associations 1 Studies 1 |
T complement factor H measurement EFO_0008097 | |||
quantification of the amount of complement factor H in a sample Associations 59 Studies 13 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |