Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6