Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs36225153 4 145160700 intron variant C/T snv 9.9E-02 3
rs1264622 1.000 0.120 6 30289159 non coding transcript exon variant C/T snv 0.13 2