Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1126671 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs1800759 0.925 0.120 4 99144358 intron variant T/G snv 0.49 4
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs3735451 7 99758352 intron variant T/C snv 0.31 1
rs4646440 7 99763247 intron variant G/A snv 5.1E-02 2
rs4646437 0.827 0.200 7 99767460 intron variant G/A snv 0.30 8