Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs6449182 0.807 0.160 4 15778830 intron variant C/G snv 0.22 6