Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 9
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 5
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 4
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs16840760 2 204118831 intergenic variant T/C snv 3.6E-02 3
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3