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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs496250 0.851 0.080 3 180909515 intron variant G/A snv 0.24 5
rs12630592 0.851 0.080 3 120049399 intron variant G/A;T snv 5
rs28383487 1.000 0.040 11 27722009 5 prime UTR variant G/T snv 1.5E-02 1
rs16856199 1.000 0.040 1 232018366 intron variant T/A snv 0.10 1