Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174536 11 61784455 non coding transcript exon variant A/C snv 0.29 3