Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1250259 1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs858519 17 7628647 intron variant T/C snv 0.46 2