rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Prospective risk of cancer and the influence of tobacco use in carriers of the p16-Leiden germline variant.
25227142
2015
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Surveillance of second-degree relatives from melanoma families with a CDKN2A germline mutation.
23897584
2013
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas.
22636603
2012
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer.
21614589
2011
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
20340136
2010
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Undifferentiated carcinoma with osteoclastic giant cells (UCOCGC) of the pancreas associated with the familial atypical multiple mole melanoma syndrome (FAMMM).
18813118
2008
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families.
18981015
2008
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
16905682
2007
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
17047042
2006
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
15146471
2004
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors.
12549483
2003
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).
10956390
2000
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas.
10398427
1999
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
The p16INK4a/CDKN2A tumor suppressor and its relatives.
9823374
1998
rs730881674
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
Neoplastic Syndromes, Hereditary
C
0.700
CausalMutation
CLINVAR
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.
7640518
1995