Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060503751 0.882 0.080 1 17028691 frameshift variant AG/- delins 4
rs1060503752 0.925 0.080 1 17023994 frameshift variant CA/- del 3
rs1060503753 0.925 0.080 1 17027790 stop gained T/A snv 3
rs1060503757 0.882 0.080 1 17024024 frameshift variant G/- delins 5
rs1060503759 0.925 0.080 1 17024013 stop gained C/T snv 3
rs1060503762 0.925 0.080 1 17044820 stop gained C/T snv 3
rs1060503763 0.925 0.080 1 17027848 stop gained A/C snv 3
rs1060503764 0.925 0.080 1 17022655 frameshift variant -/A delins 4
rs1131691049 0.882 0.080 1 17054019 start lost T/A snv 5
rs1131691055 0.925 0.080 1 17044889 splice acceptor variant C/A;T snv 4
rs1209914140 0.925 0.080 1 17022687 frameshift variant -/CGCCTCTGTGAAG delins 4.0E-06 3
rs138996609 0.882 0.080 1 17022685 missense variant G/A snv 8.0E-06 7.0E-06 5
rs1553176976 0.925 0.080 1 17018936 frameshift variant -/AGCT delins 3
rs1553176979 0.925 0.080 1 17018938 frameshift variant -/C ins 3
rs1553177436 0.925 0.080 1 17024007 frameshift variant C/- delins 3
rs1553177676 0.925 0.080 1 17027784 stop gained G/A snv 3
rs1553177678 0.925 0.080 1 17027798 frameshift variant T/- del 3
rs1553178726 0.925 0.080 1 17044756 splice region variant C/G snv 3
rs1557738304 0.925 0.080 1 17018943 frameshift variant -/C delins 3
rs1557739966 0.925 0.080 1 17024017 missense variant A/G snv 3
rs1557741425 0.925 0.080 1 17028623 frameshift variant -/C delins 3
rs200245469 0.925 0.080 1 17022724 missense variant G/A;C snv 4.0E-06 4
rs267607032 0.882 0.080 1 17028605 missense variant C/A snv 1.2E-05 2.8E-05 5
rs397516833 0.882 0.080 1 17028737 splice acceptor variant C/G snv 5
rs397516836 0.882 0.080 1 17024015 stop gained C/A;T snv 5