Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 8
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 5
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26 5