rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.
|
26104880 |
2015 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Genotype analysis in Hungarian patients with multiple primary melanoma.
|
24660985 |
2014 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
|
25780468 |
2014 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK.
|
21325014 |
2011 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs372670098
|
|
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 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes.
|
19484507 |
2009 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
rs372670098
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a.
|
9751050 |
1998 |
rs372670098
|
|
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 |