Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214