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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23