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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 10