Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42