Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45539732 0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 6
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs11714843 0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs2266959 0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs3825568 0.807 0.120 14 68793871 5 prime UTR variant C/G;T snv 6