Varaico: Literature-Extracted Genetic Variants

Gene:CDKN2A
Variant:p.H66H
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CDKN2A

NM_000077.5:p.H66H

Associated Papers

Genetic susceptibility in early-onset melanoma: An observational Greek cohort study.

Chatziioannou E et al.

Journal of the European Academy of Dermatology and Venereology : Jeadv, 2025

Uterine lavage identifies cancer mutations and increased TP53 somatic mutation burden in individuals with ovarian cancer.

Ghezelayagh TS et al.

Cancer Research Communications, 2022

36311816 (PubMed )
Supplement: crc-22-0314-s02.xlsx › Table_S6_List_of_mutations

The LOVD3 platform: efficient genome-wide sharing of genetic variants.

Fokkema IFAC et al.

European Journal of Human Genetics : Ejhg, 2021

34521998 (PubMed )
Supplement: 41431_2021_959_MOESM3_ESM.pdf

Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants.

Overbeek KA et al.

Journal of Medical Genetics, 2021

32482799 (PubMed )
Supplement: jmedgenet-2019-106562supp001.pdf

Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.

Xu H et al.

Nature Communications, 2015

Germline CDKN2A mutations among Greek patients with early-onset and multiple primary cutaneous melanoma.

Stratigos AJ et al.

The Journal of Investigative Dermatology, 2006

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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."