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
rs1801222 0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs10986018 9 98361054 intron variant T/C snv 7.9E-02 2
rs12085006 1 11898666 intergenic variant A/G;T snv 2