Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1