Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 5
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs561241
F7
13 113105720 upstream gene variant T/C;G snv 3
rs1755685 13 113102878 upstream gene variant C/A snv 0.14 1
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 1
rs776905
F10
13 113127628 intron variant A/C snv 8.7E-02 1
rs488703
F7
13 113116562 intron variant G/A snv 0.14 1
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 1
rs9390459
STXBP5
6 147359223 synonymous variant A/G snv 0.53 0.55 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 1