Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs12913832 0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs16891982 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 13
rs1800407 0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 10
rs6059655 0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs1129038 0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 8
rs1667392 15 28288419 intron variant G/A;C;T snv 2