Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs786204963
rs786204963
3 0.925 0.080 X 18588055 missense variant A/C snv 0.700 0
dbSNP: rs786204966
rs786204966
1 1.000 0.080 X 18604014 stop gained G/T snv 0.700 0
dbSNP: rs786204968
rs786204968
1 1.000 0.080 X 18604265 frameshift variant C/- del 0.700 0
dbSNP: rs786204969
rs786204969
1 1.000 0.080 X 18604299 stop gained C/T snv 0.700 0
dbSNP: rs786204970
rs786204970
1 1.000 0.080 X 18604339 frameshift variant -/A delins 0.700 0
dbSNP: rs786204972
rs786204972
1 1.000 0.080 X 18604473 frameshift variant T/- delins 0.700 0
dbSNP: rs786204975
rs786204975
1 1.000 0.080 X 18604778 frameshift variant C/- del 0.700 0
dbSNP: rs786204976
rs786204976
2 0.925 0.200 X 18608913 splice donor variant G/A snv 0.700 0
dbSNP: rs786204981
rs786204981
1 1.000 0.080 X 18628578 stop gained C/A;T snv 0.700 0
dbSNP: rs786204983
rs786204983
2 0.925 0.200 X 18579844 splice acceptor variant TAGAATATGCT/- delins 0.700 0
dbSNP: rs786204984
rs786204984
1 1.000 0.080 X 18579969 splice donor variant G/A snv 0.700 0
dbSNP: rs786204986
rs786204986
1 1.000 0.080 X 18584262 splice acceptor variant G/A snv 0.700 0
dbSNP: rs786204988
rs786204988
1 1.000 0.080 X 18584308 frameshift variant -/GT delins 0.700 0
dbSNP: rs786204989
rs786204989
1 1.000 0.080 X 18584327 missense variant G/T snv 0.700 0
dbSNP: rs786204990
rs786204990
1 1.000 0.080 X 18588058 frameshift variant -/TTTTA delins 0.700 0
dbSNP: rs786204992
rs786204992
1 1.000 0.080 X 18598575 frameshift variant A/- delins 0.700 0