G MYRF | |||
Description: myelin regulatory factor Associations 1462 Studies 689 |
G MYRF-AS1 | |||
Description: MYRF antisense RNA 1 Associations 120 Studies 85 |
V rs2071213 | |||
Location: 11:61766538 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 1 Studies 1 |
V rs11230796 | |||
Location: 11:61761795 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 4 Studies 4 |
V rs10792318 | |||
Location: 11:61763971 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 30 Studies 30 |
V rs198472 | |||
Location: 11:61759794 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 5 Studies 5 |
V rs198467 | |||
Location: 11:61766436 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 2 Studies 2 |
V rs572537530 | |||
Location: 11:61762184 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 10 Studies 10 |
V rs198476 | |||
Location: 11:61758258 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 4 Studies 4 |
V rs79519287 | |||
Location: 11:61764338 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 4 Studies 4 |
V rs198470 | |||
Location: 11:61760834 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 3 Studies 3 |
V rs61896137 | |||
Location: 11:61763028 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 3 Studies 3 |
V rs695186 | |||
Location: 11:61760455 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 3 Studies 3 |
V rs543711028 | |||
Location: 11:61758095 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF Associations 4 Studies 4 |
V rs198462 | |||
Location: 11:61756647 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 27 Studies 27 |
V rs198460 | |||
Location: 11:61757502 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 20 Studies 20 |
V rs520987 | |||
Location: 11:61753974 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 16 Studies 16 |
V rs198464 | |||
Location: 11:61754149 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 5 Studies 5 |
V rs198461 | |||
Location: 11:61756894 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 16 Studies 16 |
V rs198459 | |||
Location: 11:61757548 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 5 Studies 5 |
V rs198465 | |||
Location: 11:61753846 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): MYRF,MYRF-AS1 Associations 1 Studies 1 |
V rs174535 | |||
Location: 11:61783884 Cytogenetic region:11q12.2 Most severe consequence: Missense variant Mapped gene(s): TMEM258,MYRF Associations 263 Studies 257 |
V rs174536 | |||
Location: 11:61784455 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 124 Studies 100 |
V rs174537 | |||
Location: 11:61785208 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 156 Studies 152 |
V rs174528 | |||
Location: 11:61776027 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 62 Studies 58 |
V rs174534 | |||
Location: 11:61781986 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 70 Studies 70 |
V rs108499 | |||
Location: 11:61779765 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 117 Studies 117 |
V rs509360 | |||
Location: 11:61781087 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 106 Studies 106 |
V rs174529 | |||
Location: 11:61776489 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 58 Studies 51 |
V rs11320420 | |||
Location: 11:61774535 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 31 Studies 11 |
V rs174533 | |||
Location: 11:61781553 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 111 Studies 109 |
V rs7943728 | |||
Location: 11:61779596 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 26 Studies 26 |
V rs174530 | |||
Location: 11:61779120 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 85 Studies 85 |
V rs628993 | |||
Location: 11:61772219 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 2 Studies 2 |
V rs2956395 | |||
Location: 11:61752514 Cytogenetic region:11q12.2 Most severe consequence: Regulatory region variant Mapped gene(s): MYRF-AS1 Associations 2 Studies 2 |
V rs174532 | |||
Location: 11:61781402 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 53 Studies 53 |
V rs198421 | |||
Location: 11:61750765 Cytogenetic region:11q12.2 Most severe consequence: Intergenic variant Mapped gene(s): MYRF-AS1 Associations 23 Studies 23 |
V rs72920160 | |||
Location: 11:61780479 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 1 Studies 1 |
V rs75158668 | |||
Location: 11:61778370 Cytogenetic region:11q12.2 Most severe consequence: Splice polypyrimidine tract variant Mapped gene(s): TMEM258,MYRF Associations 2 Studies 2 |
V rs17762402 | |||
Location: 11:61785729 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 6 Studies 6 |
V rs149803 | |||
Location: 11:61771548 Cytogenetic region:11q12.2 Most severe consequence: Synonymous variant Mapped gene(s): TMEM258,MYRF Associations 1 Studies 1 |
V rs149804 | |||
Location: 11:61771134 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 5 Studies 5 |
V rs117301449 | |||
Location: 11:61780532 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 9 Studies 9 |
V rs579383 | |||
Location: 11:61769111 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 2 Studies 2 |
V rs556261560 | |||
Location: 11:61747854 Cytogenetic region:11q12.2 Most severe consequence: Tf binding site variant Mapped gene(s): MYRF-AS1 Associations 4 Studies 4 |
V rs650436 | |||
Location: 11:61768958 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 2 Studies 2 |
V rs148999057 | |||
Location: 11:61784636 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 1 Studies 1 |
V rs2269928 | |||
Location: 11:61770057 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 4 Studies 4 |
V rs198422 | |||
Location: 11:61748295 Cytogenetic region:11q12.2 Most severe consequence: Intergenic variant Mapped gene(s): MYRF-AS1 Associations 1 Studies 1 |
V rs11320420 (rs1219849860) | |||
Location: 11:61774535 Cytogenetic region:11q12.2 Most severe consequence: Intron variant Mapped gene(s): TMEM258,MYRF Associations 2 Studies 2 |
T myelin regulatory factor measurement EFO_0802767 | |||
Quantification of myelin regulatory factor in a sample. Associations 3 Studies 2 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |