Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs4820599
LRRC75B ; GGT1
0.925 0.160 22 24594246 intron variant A/G snv 0.43 6
rs11597390 10 100101678 downstream gene variant G/A snv 0.29 4
rs1780324 1 21495264 intergenic variant A/G snv 0.48 3
rs9467160
GPLD1
6 24441518 intron variant G/A snv 0.29 3
rs10761779
JMJD1C
10 63515167 intron variant A/G snv 0.42 3
rs12355784
JMJD1C
10 63361805 intron variant C/A;T snv 3