Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
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
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306