Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3835942 1.000 0.040 2 161226860 intron variant -/GGTAATAAACAACCATGAGGTCTTTTTCTTTTGTCAATATACAACGTGATTATACTGAGAAG delins 1
rs16958477 0.925 0.040 15 73926125 5 prime UTR variant A/C snv 0.33 2
rs761230732 1.000 0.040 1 11801211 missense variant A/C;G snv 4.0E-06 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs4886425 1.000 0.040 15 73832202 intergenic variant A/G snv 0.71 2
rs16958382 1.000 0.040 15 73847349 intergenic variant A/G snv 5.6E-02 1
rs4338750 1.000 0.040 15 73857246 intergenic variant A/G snv 0.51 1
rs723434 1.000 0.040 15 74050989 downstream gene variant A/G snv 0.19 1
rs746655 1.000 0.040 15 73815336 intergenic variant A/G snv 0.72 1
rs216541 1.000 0.040 2 32130481 non coding transcript exon variant A/G;T snv 1
rs7173049 1.000 0.040 15 73952269 downstream gene variant A/G;T snv 1
rs7803992 1.000 0.040 7 147343905 intron variant A/G;T snv 1
rs12594472 1.000 0.040 15 73934799 intron variant A/T snv 8.4E-02 1
rs999743 1.000 0.040 15 73822628 regulatory region variant A/T snv 0.15 1
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3784556
PML
1.000 0.040 15 74039847 intron variant C/A;G;T snv 1
rs7137828 0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs4445847 1.000 0.040 15 73879672 intron variant C/A;T snv 1
rs893816 1.000 0.040 15 73936123 intron variant C/A;T snv 1
rs1992314 0.925 0.040 15 73931426 intron variant C/G snv 0.29 2
rs1550437 1.000 0.040 15 73928957 intron variant C/T snv 0.31 1
rs16958494 1.000 0.040 15 73939008 intron variant C/T snv 3.6E-02 1
rs3522 1.000 0.040 15 73952003 3 prime UTR variant C/T snv 0.48 1