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
rs4737010 8 41772929 intron variant G/A snv 0.32 6
rs1354034 3 56815721 intron variant T/C snv 0.49 4
rs549579958 17 76387027 frameshift variant G/- del 1.8E-03 2