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
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs1805008 0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16
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
rs1805005 0.827 0.080 16 89919436 missense variant G/T snv 8.6E-02 8.0E-02 8
rs1042602 0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 6
rs12931267 1.000 0.040 16 89752324 intron variant C/G snv 4.7E-02 4
rs1110400 1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 3