Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs7958904 0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15