Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
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
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs11075992
FTO
1.000 0.080 16 53786154 intron variant T/C snv 0.41 3
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs115460205
FSTL5
1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 1
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs1316543
GRK5
1.000 0.080 10 119445148 intron variant G/A snv 0.15 3
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4