Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 3
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 2
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 1
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 2
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 2
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs2293855
MTMR9
0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 1
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs481843
LINC02702
1.000 0.040 11 116655150 non coding transcript exon variant C/T snv 8.8E-02 4
rs486394
LINC02702
1.000 0.040 11 116655605 intron variant A/C;T snv 3
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3