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
rs630014
ABO
9 133274306 intron 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
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
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 3
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3