Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11104881 12 88449697 intergenic variant T/A;C snv 1
rs1347767 2 135728087 downstream gene variant C/T snv 0.97 1
rs1917445 11 103718366 intron variant C/T snv 0.44 1
rs272594 8 80557885 upstream gene variant A/C snv 0.22 1
rs2994007 1 36415228 downstream gene variant G/A;C snv 1
rs34733715 19 51376740 upstream gene variant G/A snv 0.23 1
rs35272691 17 40001588 downstream gene variant T/A;C snv 1
rs546829 4 74090655 upstream gene variant A/T snv 0.63 1
rs6936204 0.925 0.160 6 32249315 intergenic variant T/C snv 0.70 1
rs79208462 12 109660467 downstream gene variant A/G snv 8.7E-04 1
rs562760
ATXN1
6 16749780 intron variant G/C;T snv 0.55 1
rs5013026
BCL2L13
22 17688884 intron variant C/T snv 0.51 1
rs75418630
CCDC26
8 129544786 intron variant A/G snv 1.8E-03 1
rs4237036
CHD7
8 60788498 intron variant C/T snv 0.52 1
rs6775745
CPNE4
3 132095056 intron variant G/A;T snv 1
rs886816
CREB5
7 28683790 intron variant G/A snv 0.22 1
rs149881318
DARS1
2 135938202 intron variant T/C snv 5.5E-03 1
rs2837828
DSCAM
21 40803034 intron variant A/G snv 0.44 1
rs2301813
GRIN3B
19 1000800 synonymous variant G/C snv 0.71 0.68 1
rs115681968
HLA-B ; LOC112267902
6 31304776 intron variant G/A snv 1
rs10171849
IL1RN
2 113108257 intron variant A/C snv 0.35 1
rs7587928
KIDINS220
2 8808940 intron variant T/C snv 0.29 1
rs12606438
LINC01478
18 44461098 intron variant A/C snv 0.11 1
rs4804815
LOC105372263
19 7777783 intergenic variant C/G snv 0.19 1
rs12469306
LY75 ; LY75-CD302
2 159848974 intron variant A/G snv 0.87 1