Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10506346 12 56937074 upstream gene variant G/A snv 0.12 1
rs10902094 11 1119225 intergenic variant G/A;C snv 1
rs112068732 17 40204213 regulatory region variant A/G snv 3.9E-02 1
rs11255938 10 8808772 intergenic variant C/T snv 0.34 1
rs113660049 19 9026584 intergenic variant G/A snv 0.28 1
rs1420466 3 169000309 upstream gene variant T/A;G snv 1
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1
rs2486294 10 8245634 regulatory region variant G/C;T snv 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs4713841 6 35189310 intergenic variant T/C snv 0.28 1
rs56147623 2 102553704 intergenic variant G/A snv 3.6E-02 1
rs61957178 13 73421057 intron variant C/T snv 0.19 1
rs6473228 8 80387531 intron variant G/T snv 0.59 1
rs7091181 10 8471661 upstream gene variant G/A;C snv 1
rs802731 6 127958284 intergenic variant C/G;T snv 1
rs9494892 6 137902352 intron variant G/T snv 6.2E-02 1
rs9611602
ACO2
22 41512401 intron variant T/C snv 0.19 1
rs7170165
ADAMTSL3
15 83878087 intron variant A/C;G snv 1
rs12190426
AHI1
6 135391300 intron variant G/A snv 0.15 1
rs72925996
BACH2
6 90220794 intron variant T/A;C snv 1
rs112119265
CARD11
7 3022995 intron variant T/G snv 5.2E-02 1
rs112204664
CASC15
6 21867474 intron variant G/A snv 0.13 1
rs2949669
CD247
1 167448647 intron variant C/G;T snv 1
rs3744787
CEP295NL ; TIMP2
17 78897589 non coding transcript exon variant A/G snv 0.28 1
rs9603608
COG6
13 39744682 intron variant A/C snv 0.30 1