Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 3
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 2
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 2
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 2
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 2
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 2
rs13069000 3 66748526 regulatory region variant C/G snv 0.15 1
rs7084402 0.925 0.040 10 58505644 intergenic variant A/G snv 0.51 1
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 1
rs11868441
BCAS3
17 61161860 intron variant A/G snv 0.62 1
rs219778
CLDN14 ; LOC105369301
0.925 0.120 21 36462343 intron variant A/G snv 0.31 1
rs2049805
GBAP1
1 155225189 intron variant T/A;C snv 1
rs6026584
GNAS
0.925 0.040 20 58894018 intron variant T/C snv 0.70 1
rs1169286
HNF1A
1.000 0.080 12 120981253 intron variant T/C snv 0.39 1
rs10767873
LOC101928338
11 30747131 intergenic variant C/T snv 0.35 1
rs10937329
LOC107986166
3 187995930 downstream gene variant T/A snv 0.27 1
rs16853722
MECOM
3 169432844 intron variant T/C snv 0.11 1
rs11123170
PAX8 ; PAX8-AS1
2 113221363 intron variant C/G snv 0.35 1
rs7227483
SLC14A2 ; LOC107985153
18 45607165 intron variant A/G;T snv 1