Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10