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
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs2488457 0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs7234029 0.807 0.320 18 12877061 intron variant A/G snv 0.27 7