Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 5
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs11597390 10 100101678 downstream gene variant G/A snv 0.29 4
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs13077101
RABL3
3 120706484 intron variant T/C snv 4
rs16840760 2 204118831 intergenic variant T/C snv 3.6E-02 4
rs2078087
NMNAT2
1 183389270 intron variant C/T snv 0.16 4
rs892295
CHL1
3 355870 intron variant A/G snv 0.87 4
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3