Source: GWASCAT ×
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 55
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 6
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 3
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 2
rs488703
F7
13 113116562 intron variant G/A snv 0.14 2
rs6532796
LOC100507053
1.000 0.040 4 99121091 intron variant A/G;T snv 2
rs12477385
SCN2A
2 165288340 intron variant G/T snv 0.20 2
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 2
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 2
rs113773825 16 47003958 upstream gene variant A/T snv 1.0E-02 1
rs1149606 11 76779014 upstream gene variant G/A snv 0.13 1
rs1755685 13 113102878 upstream gene variant C/A snv 0.14 1
rs35866503 7 73591446 downstream gene variant C/T snv 0.15 1
rs72873804 18 5947039 intron variant G/C;T snv 4.6E-02 1
rs9805933 14 44551736 intron variant A/C snv 0.32 1
rs56317999
DSN1
20 36757832 intron variant G/A snv 2.2E-02 1
rs474671
F10
13 113121904 upstream gene variant T/C snv 0.15 1
rs776905
F10
13 113127628 intron variant A/C snv 8.7E-02 1
rs561241
F7
13 113105720 upstream gene variant T/C;G snv 1
rs569557
F7
13 113115603 intron variant G/A snv 0.12 1
rs498475
JAZF1-AS1
7 28216621 intron variant G/A snv 0.49 1
rs1046205
MCF2L
13 113097743 3 prime UTR variant A/T snv 0.22 1