Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14