Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs13077101
RABL3
3 120706484 intron variant T/C snv 4
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3
rs4896310
LOC105378021
1.000 0.120 6 138018697 intergenic variant A/G;T snv 3
rs4949718
ST6GALNAC3
1 76433779 intron variant T/A;C snv 3
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/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
rs1658972 9 6665010 intron variant C/A;T snv 2
rs185355701
LOC105375026 ; LINC01016
6 33893066 intron variant G/A;T snv 2
rs200088103
GPT ; LOC101928953
8 144505033 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.0E-04 2
rs201022 6 6669940 intergenic variant C/A;T snv 2
rs2383733 9 27869512 intergenic variant A/G;T snv 2
rs4979372
AKNA
9 114377802 intron variant T/C;G snv 2
rs7803882 7 55869748 intergenic variant T/A;C snv 2
rs8108722 19 10236408 intergenic variant T/A;C snv 2
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3