Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33