Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1283377907 1.000 0.120 16 88842829 missense variant T/A snv 1.2E-05 7.0E-06 1
rs1288687291 1.000 0.120 16 88843167 synonymous variant T/C snv 7.4E-06 1
rs1296755011 1.000 0.120 16 88842799 missense variant C/T snv 4.0E-06 1
rs1301146300 1.000 0.120 16 88837721 missense variant A/C snv 4.0E-06 1
rs1301198698 1.000 0.120 16 88837690 missense variant G/C snv 1
rs1303492021 1.000 0.120 16 88814510 missense variant C/T snv 7.0E-06 1
rs1308500116 1.000 0.120 16 88837722 missense variant A/G snv 1.2E-05 1
rs1401175486 1.000 0.120 16 88818009 missense variant T/A;C snv 1
rs141340188 1.000 0.120 16 88841965 missense variant G/A;T snv 8.2E-06 1
rs1421990673 1.000 0.120 16 88842792 missense variant G/A snv 4.0E-06 1
rs1444754604 1.000 0.120 16 88841068 missense variant C/T snv 8.0E-06 7.0E-06 1
rs145798311 1.000 0.120 16 88842769 missense variant G/A snv 4.0E-05 4.2E-05 1
rs146093755 1.000 0.120 16 88840999 missense variant C/T snv 8.0E-06 3.5E-05 1
rs150734270 1.000 0.120 16 88826714 missense variant C/T snv 1.8E-03 1.7E-03 1
rs1567526805 1.000 0.120 16 88832000 stop gained G/A snv 1
rs1567538216 1.000 0.120 16 88842831 splice acceptor variant T/C snv 1
rs191519947 1.000 0.120 16 88842807 missense variant A/C;G snv 4.8E-05; 3.3E-04 1
rs199638097 1.000 0.120 16 88842811 missense variant C/T snv 1.6E-05 7.0E-06 1
rs200374326 1.000 0.120 16 88841083 stop gained G/A snv 1.6E-05 2.8E-05 1
rs267606838 1.000 0.120 16 88826822 missense variant C/T snv 1
rs398123433 1.000 0.120 16 88814488 missense variant C/A snv 1.4E-05 1
rs398123438 1.000 0.120 16 88837725 missense variant C/T snv 2.8E-05 2.1E-05 1
rs398123439 1.000 0.120 16 88837711 stop gained C/T snv 8.0E-06 7.0E-06 1
rs398123440 1.000 0.120 16 88835779 missense variant G/A;T snv 2.0E-05; 4.0E-06 1
rs537013895 1.000 0.120 16 88832048 missense variant T/A;C snv 7.6E-05 2.1E-05 1