Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 2
rs7221109 0.925 0.160 17 40614034 intergenic variant T/C snv 0.69 2
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs16956936
DNAH2
1.000 0.120 17 7730374 intron variant C/A;T snv 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 3
rs12599402
CLEC16A
0.925 0.160 16 11096031 intron variant T/C snv 0.51 2
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs13330041
CLEC16A
1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs17673553
CLEC16A
1.000 0.120 16 11148049 intron variant A/G snv 0.18 2
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 2
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 2
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs12444268 1.000 0.120 16 20331250 upstream gene variant T/A snv 0.22 1
rs12923849
CLEC16A
1.000 0.120 16 10968140 intron variant G/A snv 0.13 1
rs12931878
CLEC16A
1.000 0.120 16 10948337 intron variant A/G snv 0.14 1
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16 1