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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35