Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs1285136498 0.807 0.080 5 143400101 missense variant G/A snv 13
rs4987188 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs2016347 0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs1288373809 0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs438034 0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4