Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31