Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9912300 0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs2304497 1.000 0.080 17 41909521 missense variant T/C;G snv 4.0E-06; 0.10 0.11 1