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: rs587781338
rs587781338
1.000 0.120 1 45332080 stop gained G/A snv 1.2E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2005 2014
dbSNP: rs587782243
rs587782243
0.882 0.080 1 17033060 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2010 2012
dbSNP: rs748170941
rs748170941
1.000 0.120 1 45333452 stop gained C/G;T snv 4.0E-06; 4.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2005 2015
dbSNP: rs762307622
rs762307622
1.000 0.120 1 45332955 stop gained C/A;T snv 5.6E-05 2.1E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2015 2017
dbSNP: rs797044973
rs797044973
FH
0.925 0.320 1 241504246 splice acceptor variant C/G;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2005 2005
dbSNP: rs863223973
rs863223973
FH
1.000 0.200 1 241504127 missense variant A/C;G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2010 2014
dbSNP: rs863223980
rs863223980
FH
0.925 0.320 1 241517310 stop gained G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2002 2015
dbSNP: rs863224000
rs863224000
FH
1.000 0.200 1 241504216 missense variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 1998 2011
dbSNP: rs863224002
rs863224002
FH
1.000 0.200 1 241504203 missense variant G/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2011 2012
dbSNP: rs864621967
rs864621967
1 45331176 splice donor variant AGTGCCT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2001 2002
dbSNP: rs864622450
rs864622450
1 45333158 missense variant T/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2009 2010
dbSNP: rs876658461
rs876658461
0.827 0.200 1 17023975 stop gained G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2007 2009
dbSNP: rs876659329
rs876659329
1.000 0.040 1 17044767 missense variant A/G;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2003 2015
dbSNP: rs876659330
rs876659330
1 17044758 splice region variant C/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2003 2015
dbSNP: rs878854576
rs878854576
1.000 0.080 1 17028727 missense variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2006 2009
dbSNP: rs886039368
rs886039368
FH
1.000 0.160 1 241497861 stop gained C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2011 2011
dbSNP: rs1131691060
rs1131691060
1 17027866 splice acceptor variant C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2003 2003
dbSNP: rs1131691062
rs1131691062
1 161323612 splice acceptor variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2009 2009
dbSNP: rs1131691240
rs1131691240
FH
1 241512145 splice acceptor variant T/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2011 2011
dbSNP: rs1131691244
rs1131691244
FH
1 241500571 missense variant G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2006 2006
dbSNP: rs1131691245
rs1131691245
FH
1 241497922 stop gained G/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2011 2011
dbSNP: rs1228560456
rs1228560456
1 17023981 missense variant G/A;C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2005 2005
dbSNP: rs1553125075
rs1553125075
1 45331255 frameshift variant TG/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2001 2001
dbSNP: rs1553130185
rs1553130185
1.000 0.120 1 45333453 stop gained C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2005 2005
dbSNP: rs1553177290
rs1553177290
1 17022720 missense variant C/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2006 2006