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
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1060501201 0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs267605077 0.925 0.080 17 7675212 missense variant A/G;T snv 3
rs138983188 0.925 0.080 17 7674863 missense variant G/A;T snv 4.0E-06 2
rs143458271 0.925 0.080 17 7676589 synonymous variant C/T snv 9.2E-05 8.4E-05 2