Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1210554604
HTT
1.000 0.120 4 3131662 missense variant G/A snv 1
rs13102260 1.000 0.120 4 3074678 intron variant G/A snv 0.15 1
rs1313770 1.000 0.120 4 3056082 intron variant A/G snv 0.57 1