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
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9