Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs3027012 1 159204333 5 prime UTR variant C/T snv 0.13 3
rs863002 1 159205130 intron variant C/T snv 0.28 2
rs863006 1 159207958 non coding transcript exon variant G/A snv 0.56 1
rs3027001 1.000 0.040 1 159199673 intron variant C/G;T snv 1