Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
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
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
rs13395911
EFHD1
2 232655544 intron variant A/T snv 0.59 3
rs1583686 5 85922051 intergenic variant T/C snv 0.79 3
rs1998303 9 82800066 intergenic variant A/G snv 0.37 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3
rs4949718
ST6GALNAC3
1 76433779 intron variant T/A;C snv 3
rs74913549
PANX1
11 94180526 intron variant T/A;C snv 3
rs9937036 16 16636871 intron variant T/A;C;G snv 3
rs10787429
GPAM
10 112189906 intron variant T/A;C snv 2
rs11124554
STRN
2 36922355 intron variant T/A;C snv 2
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02 2
rs13247499
JAZF1
7 28139639 intron variant C/A snv 0.10 2
rs144983009 5 56792072 intergenic variant C/T snv 5.7E-02 2