Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs624601
ABO
9 133259961 intron variant G/A snv 0.28 3
rs613423
ABO
9 133260074 intron variant G/A snv 0.27 3
rs574347
ABO
9 133260255 intron variant T/C snv 0.27 3
rs579483
ABO
9 133260793 intron variant T/A snv 3
rs579622
ABO
9 133260839 intron variant G/A snv 3
rs493211
ABO
9 133261113 intron variant G/A snv 1
rs688976
ABO
9 133261367 missense variant C/A snv 3
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
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs9411488 9 133278802 upstream gene variant G/T snv 0.34 2
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
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