Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 5
rs1545747
MEGF11
15 66164979 intron variant G/T snv 0.97 3
rs17369571 13 21913486 intergenic variant G/A snv 0.20 1
rs1917805 10 49597937 intergenic variant A/G snv 0.41 1
rs2019023 19 54547968 upstream gene variant A/C;G;T snv 1
rs35019477 9 116409871 intergenic variant AC/-;ACAC;ACACAC;ACACACAC delins 1
rs35803309
DNAH11
7 21683510 intron variant -/T delins 0.13 1
rs6743376
IL1F10
2 113074756 missense variant C/A snv 0.69 0.69 1
rs116621133
KANK4
1 62296579 intron variant T/A snv 4.5E-03 1
rs12452028
SLC26A11
17 80238432 intron variant G/C snv 0.31 1
rs146151667
SPAG16
2 214319145 intron variant A/G snv 8.0E-03 1