Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs786201161
rs786201161
0.882 0.080 1 17024076 splice acceptor variant T/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 2007 2016
dbSNP: rs786203115
rs786203115
0.925 0.120 1 45332300 stop gained G/A snv 1.6E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 2007 2015
dbSNP: rs863224015
rs863224015
FH
1.000 0.160 1 241511983 missense variant T/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 2002 2013
dbSNP: rs1060503757
rs1060503757
0.882 0.080 1 17024024 frameshift variant G/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2005 2009
dbSNP: rs1060503764
rs1060503764
0.925 0.080 1 17022655 frameshift variant -/A delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2005 2009
dbSNP: rs1553341942
rs1553341942
FH
0.925 0.320 1 241517209 frameshift variant -/T delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2006 2016
dbSNP: rs199989617
rs199989617
1.000 0.120 1 45332574 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2008 2015
dbSNP: rs376561094
rs376561094
1.000 0.120 1 45332636 stop gained G/A snv 4.0E-06 7.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2006 2009
dbSNP: rs398123159
rs398123159
FH
0.925 0.320 1 241504130 missense variant A/T snv 1.2E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2003 2011
dbSNP: rs398123166
rs398123166
FH
0.925 0.320 1 241508781 stop gained G/A;C;T snv 4.0E-06; 4.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2003 2012
dbSNP: rs587781266
rs587781266
0.925 0.080 1 17022654 frameshift variant GAGA/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2002 2007
dbSNP: rs587781270
rs587781270
0.882 0.080 1 17033058 splice donor variant A/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2006 2012
dbSNP: rs786201063
rs786201063
0.882 0.080 1 17033059 splice donor variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2006 2007
dbSNP: rs786201316
rs786201316
0.925 0.080 1 17028712 frameshift variant T/CC delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2006 2015
dbSNP: rs786205147
rs786205147
0.882 0.120 1 161340638 missense variant G/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2009 2016
dbSNP: rs876660446
rs876660446
FH
1.000 0.080 1 241502559 missense variant G/A;T snv 4.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2011 2014
dbSNP: rs1060499635
rs1060499635
FH
1.000 0.160 1 241508758 inframe deletion TGCTGT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2013 2014
dbSNP: rs1060499639
rs1060499639
FH
1 241506084 missense variant C/G;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2011 2012
dbSNP: rs1131691238
rs1131691238
FH
1 241504056 missense variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2012 2014
dbSNP: rs11545654
rs11545654
FH
1.000 0.200 1 241512085 missense variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 1998 2011
dbSNP: rs1278834014
rs1278834014
1 17023973 missense variant C/A;G;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2006 2015
dbSNP: rs1553125243
rs1553125243
1.000 0.120 1 45331302 frameshift variant T/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2007 2017
dbSNP: rs1553136984
rs1553136984
1 45340218 splice donor variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2006 2007
dbSNP: rs398123163
rs398123163
FH
0.925 0.320 1 241500534 frameshift variant T/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2007 2011
dbSNP: rs587776653
rs587776653
0.827 0.160 1 161356841 splice donor variant G/A;C;T snv 8.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2003 2005