Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs7195830 0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs200340021 0.925 0.080 12 14882204 missense variant C/T snv 7.0E-06 3