Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs117068593
RIN3
14 92651884 missense variant C/T snv 0.13 0.11 4
rs13116999
LOC105377462
4 144521212 intron variant G/A snv 0.65 4
rs1496255 4 120683279 downstream gene variant G/A;T snv 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs7424771
RBMS1
2 160419867 intron variant G/A snv 0.44 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12 3
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs1047912
DIP2B
12 50745079 3 prime UTR variant C/T snv 0.21 3
rs10998018
MYPN
10 68203197 intron variant G/A snv 0.41 3
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11176001 12 66015587 regulatory region variant C/A snv 9.6E-02 3
rs11191841
STN1
10 103879853 3 prime UTR variant T/C snv 0.47 3
rs11621587
RIN3
14 92631994 intron variant G/C;T snv 3
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 3
rs117642368 17 45321692 upstream gene variant G/C snv 6.9E-02 3
rs12096239
DHDDS
1 26470431 3 prime UTR variant G/C snv 0.23 3
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 3
rs12331869 4 55145982 intergenic variant A/G snv 0.76 3