Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27