Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17