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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs3194051 0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4