Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8