G HHIP | |||
Description: hedgehog interacting protein Associations 246 Studies 175 |
G HHIP-AS1 | |||
Description: HHIP antisense RNA 1 Associations 182 Studies 95 |
P Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A. | |||
van der Plaat DA et al. 2016 J Allergy Clin Immunol PMID:27612410 Associations 3 Studies 1 |
P Variants associated with <i>HHIP</i> expression have sex-differential effects on lung function. | |||
Fawcett KA et al. 2020 Wellcome Open Res PMID:33728380 Associations 0 Studies 4 |
V rs6854783 | |||
Location: 4:144721927 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 3 Studies 3 |
V rs1492820 | |||
Location: 4:144728869 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 3 Studies 3 |
V rs11727676 | |||
Location: 4:144737912 Cytogenetic region:4q31.21 Most severe consequence: Synonymous variant Mapped gene(s): HHIP Associations 70 Studies 68 |
V rs6537307 | |||
Location: 4:144680711 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 3 Studies 3 |
V rs2131354 | |||
Location: 4:144678756 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 15 Studies 15 |
V rs34701002 | |||
Location: 4:144669806 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs75686861 | |||
Location: 4:144700176 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 10 Studies 10 |
V rs11946517 | |||
Location: 4:144678382 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 6 Studies 6 |
V rs982903 | |||
Location: 4:144665307 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs35135458 | |||
Location: 4:144735742 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs72718211 | |||
Location: 4:144742646 Cytogenetic region:4q31.21 Most severe consequence: 3 prime utr variant Mapped gene(s): HHIP Associations 5 Studies 5 |
V rs55817790 | |||
Location: 4:144734237 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 3 Studies 3 |
V rs6826012 | |||
Location: 4:144737134 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 2 Studies 2 |
V rs2575580 | |||
Location: 4:144683873 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 2 Studies 2 |
V rs74730596 | |||
Location: 4:144706819 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs141349721 | |||
Location: 4:144684062 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs1492819 | |||
Location: 4:144698261 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs77362667 | |||
Location: 4:144670142 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs6812830 | |||
Location: 4:144692655 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs6817771 | |||
Location: 4:144705262 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs1389029 | |||
Location: 4:144717026 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs6827641 | |||
Location: 4:144732542 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs117072351 | |||
Location: 4:144676679 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs6537302 | |||
Location: 4:144666964 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs13131837 | |||
Location: 4:144693832 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs11733546 | |||
Location: 4:144733744 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs12507436 | |||
Location: 4:144691399 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs7666450 | |||
Location: 4:144741690 Cytogenetic region:4q31.21 Most severe consequence: 3 prime utr variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs1812175 | |||
Location: 4:144653692 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 32 Studies 20 |
V rs7689420 | |||
Location: 4:144647200 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 16 Studies 13 |
V rs12507427 | |||
Location: 4:144646319 Cytogenetic region:4q31.21 Most severe consequence: 5 prime utr variant Mapped gene(s): HHIP,HHIP-AS1 Associations 2 Studies 2 |
V rs114633728 | |||
Location: 4:144659020 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs7675744 | |||
Location: 4:144650894 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 4 Studies 4 |
V rs74369295 (rs147015513) | |||
Location: 4:144647693 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs1844428 | |||
Location: 4:144653044 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs13146972 | |||
Location: 4:144648540 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs2035742 | |||
Location: 4:144656218 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 2 Studies 2 |
V rs1355601 | |||
Location: 4:144659138 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs114674837 | |||
Location: 4:144660761 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs199910112 | |||
Location: 4:144646162 Cytogenetic region:4q31.21 Most severe consequence: 5 prime utr variant Mapped gene(s): HHIP,HHIP-AS1 Associations 1 Studies 1 |
V rs6845999 | |||
Location: 4:144644674 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 5 Studies 5 |
V rs12504213 | |||
Location: 4:144801156 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs201461344 | |||
Location: 4:144645095 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 1 Studies 1 |
V rs13106087 | |||
Location: 4:144645712 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 3 Studies 3 |
V rs116216151 | |||
Location: 4:144798097 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 2 Studies 2 |
V rs75385537 | |||
Location: 4:144784918 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 2 Studies 2 |
V rs4576021 | |||
Location: 4:144792617 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 3 Studies 3 |
V rs180762722 | |||
Location: 4:144764516 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs11944404 | |||
Location: 4:144749719 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 5 Studies 3 |
V rs2353940 | |||
Location: 4:144819746 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 6 Studies 6 |
V rs7680661 | |||
Location: 4:144643964 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 8 Studies 6 |
V rs13125694 | |||
Location: 4:144645696 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 9 Studies 9 |
V rs6537315 | |||
Location: 4:144803560 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs11933087 | |||
Location: 4:144801710 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 6 Studies 6 |
V rs35695619 (rs200995462) | |||
Location: 4:144691401 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs11398510 (rs568298987) | |||
Location: 4:144703215 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs191473307 | |||
Location: 4:144774201 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs2353939 | |||
Location: 4:144808572 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 3 Studies 3 |
V rs138811966 | |||
Location: 4:144797710 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs7684268 | |||
Location: 4:144792540 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs35356684 (rs762527406) | |||
Location: 4:144690785 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP Associations 1 Studies 1 |
V rs771956348 | |||
Location: 4:144814773 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs142624835 | |||
Location: 4:144811123 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs4835192 | |||
Location: 4:144817245 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs4835186 | |||
Location: 4:144765995 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs1355603 | |||
Location: 4:144645325 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP-AS1 Associations 2 Studies 2 |
V rs10029786 | |||
Location: 4:144789951 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs113268581 | |||
Location: 4:144768705 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 1 Studies 1 |
V rs13141641 | |||
Location: 4:144585304 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 22 Studies 20 |
V rs2353398 | |||
Location: 4:144601606 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs1542726 | |||
Location: 4:144594617 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 5 Studies 5 |
V rs7670758 | |||
Location: 4:144590723 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs6537297 | |||
Location: 4:144580877 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 3 Studies 3 |
V rs10029430 | |||
Location: 4:144577260 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs6537298 | |||
Location: 4:144585719 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 3 Studies 3 |
V rs1489765 | |||
Location: 4:144595226 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 3 Studies 3 |
V rs11724319 | |||
Location: 4:144589888 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs17019496 | |||
Location: 4:144577876 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs11947381 | |||
Location: 4:144616698 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs2575570 | |||
Location: 4:144627781 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs10013495 | |||
Location: 4:144584486 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs62346126 | |||
Location: 4:144639014 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 4 Studies 4 |
V rs34377763 | |||
Location: 4:144627787 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 4 Studies 4 |
V rs17776795 | |||
Location: 4:144623684 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs11407396 | |||
Location: 4:144595586 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs2942220 | |||
Location: 4:144621722 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs11100862 | |||
Location: 4:144636499 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs2175586 | |||
Location: 4:144575789 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs76722643 | |||
Location: 4:144586805 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs2353397 | |||
Location: 4:144596426 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 4 Studies 4 |
V rs13125844 | |||
Location: 4:144612792 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs10023833 | |||
Location: 4:144600037 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 3 Studies 3 |
V rs1994812 | |||
Location: 4:144601511 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs977720 | |||
Location: 4:144613703 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs7700244 | |||
Location: 4:144592027 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs138811966 (rs757932380) | |||
Location: 4:144797710 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): HHIP,ANAPC10 Associations 2 Studies 2 |
V rs13327924 | |||
Location: 4:144616596 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs570992006 | |||
Location: 4:144595679 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs7692554 | |||
Location: 4:144615184 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs2883154 | |||
Location: 4:144610693 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs6814581 | |||
Location: 4:144635074 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs56095409 | |||
Location: 4:144604255 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs4835181 | |||
Location: 4:144608442 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs12711419 | |||
Location: 4:144616094 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs34792358 | |||
Location: 4:144628816 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs72733520 | |||
Location: 4:144626033 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 2 Studies 2 |
V rs34939090 | |||
Location: 4:144641379 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs189056607 | |||
Location: 4:144628597 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs184161859 | |||
Location: 4:144601358 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
V rs1398244 | |||
Location: 4:144641305 Cytogenetic region:4q31.21 Most severe consequence: Intron variant Mapped gene(s): KRT18P51,HHIP-AS1 Associations 1 Studies 1 |
G HHIPL2 | |||
Description: HHIP like 2 Associations 5 Studies 5 |
G HHIPL1 | |||
Description: HHIP like 1 Associations 49 Studies 46 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |