Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 5
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 5
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs643434
ABO
9 133266942 intron variant A/G;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs4253417
F11
4 186277851 intron variant T/C;G snv 2
rs4253421
F11
4 186283783 intron variant A/C;G;T snv 2
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 2
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 2
rs10746487 1 9278630 intergenic variant T/A;C snv 1
rs1209731
NME7
1 169355555 intron variant T/C;G snv 1
rs12450494 17 7304568 upstream gene variant T/A;C snv 1
rs12473559
CPO
2 206828392 intron variant A/G;T snv 1
rs141325867
PSMC3
11 47422103 intron variant C/A;T snv 1
rs143478537
VBP1
X 155195893 upstream gene variant G/C;T snv 1
rs146033545
PHF21A
11 46072184 intron variant T/A;G snv 1
rs148268781 11 50663948 intergenic variant T/A;C snv 1