Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7804372 0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17