Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3