rs104894094
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
|
25645574 |
2015 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation.
|
11556834 |
2001 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CDKN2A mutations in multiple primary melanomas.
|
9516223 |
1998 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.
|
23190892 |
2013 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma.
|
21801156 |
2011 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.
|
11815963 |
2002 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
|
9699728 |
1998 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
GESPA: classifying nsSNPs to predict disease association.
|
26206375 |
2015 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CDKN2A germline mutations in individuals with cutaneous malignant melanoma.
|
17218939 |
2007 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling.
|
21150883 |
2011 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.
|
9425228 |
1998 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Novel CDKN2A mutation detected in Spanish melanoma pedigree.
|
20653773 |
2010 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma.
|
21893440 |
2011 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.
|
26681309 |
2016 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.
|
22841127 |
2012 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Role of key-regulator genes in melanoma susceptibility and pathogenesis among patients from South Italy.
|
19799798 |
2009 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutations in CDKN2A are infrequent in female patients with melanoma and breast cancer.
|
19571771 |
2009 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.
|
12700603 |
2003 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
|
25780468 |
2014 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.
|
19260062 |
2009 |
rs45476696
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.
|
11815963 |
2002 |