Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 4
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10965212
CDKN2B-AS1
0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 3
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 3
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 3
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 3
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs6698843
CELSR2
0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 3
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 3
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 2
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 2