Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 8
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 7