Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs757333753 0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6