Varaico: Literature-Extracted Genetic Variants

Gene:CCND1
Variant:p.V109G
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CCND1

NM_053056.3:p.V109G

Associated Papers

MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism.

Alvelos MI et al.

European Journal of Endocrinology, 2013

Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario.

Briollais L et al.

Bmc Medicine, 2007

SNP-SNP interactions in breast cancer susceptibility.

Onay VU et al.

Bmc Cancer, 2006

Association between the V109G polymorphism of the p27 gene and the risk and progression of oral squamous cell carcinoma.

Li G et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2004

Contribution of Cyclin-dependent Kinase Inhibitor 1B Genotypes to Childhood Leukemia Risk.

Pei JS et al.

In Vivo (athens, Greece), 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."