Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107