Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
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
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 6
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 6
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5
rs60942712 0.882 0.120 3 88998609 intergenic variant G/T snv 7.9E-02 5
rs7654093 0.882 0.120 4 154623920 upstream gene variant A/T snv 0.27 5
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs72798544
COX7A2L
0.882 0.120 2 42372465 intron variant T/G snv 1.3E-02 5
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 5
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5