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 55
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10761731 10 63267850 intron variant A/T snv 0.38 6