Disease: Venous Thrombosis
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
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
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
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
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
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs514708
ABO
9 133258352 intron variant C/T snv 0.29 4
rs626035
ABO
9 133259603 intron variant T/G snv 0.28 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs8176714
ABO
9 133257791 intron variant G/A snv 0.26 4
rs2073827
ABO
9 133261730 intron variant G/C snv 3
rs502361 9 133280016 upstream gene variant G/C snv 0.26 3
rs568203
ABO
9 133276029 upstream gene variant C/A;G snv 3