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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
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
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 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
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8