Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
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
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
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
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
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
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 10
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 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
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 7
rs7654093 0.882 0.120 4 154623920 upstream gene variant A/T snv 0.27 6