Varaico: Literature-Extracted Genetic Variants

Gene:ZNF350
Variant:p.S472P
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ZNF350

NM_021632.4:p.S472P

Associated Papers

Association between XRCC2 Arg188His Polymorphism and Breast Cancer Susceptibility: A Systematic Review and Meta-Analysis.

Dastgheib SA et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2024

Correlation between ZBRK1/ZNF350 gene polymorphism and breast cancer.

Wu J et al.

Bmc Medical Genomics, 2021

Functional Evaluation of ZNF350 Missense Genetic Variants Associated with Breast Cancer Susceptibility.

Zhang N et al.

Dna and Cell Biology, 2018

Five zinc finger protein 350 single nucleotide polymorphisms and the risks of breast cancer: a meta-analysis.

Zeng YF et al.

Oncotarget, 2017

Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.

Sigurdson AJ et al.

Radiation Research, 2009

Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families.

Desjardins S et al.

International Journal of Cancer, 2008

Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses.

García-Closas M et al.

Human Genetics, 2006

Genetic variation and willingness to participate in epidemiologic research: data from three studies.

Bhatti P et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2005

Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes.

Sigurdson AJ et al.

Bmc Cancer, 2004

Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals.

Rutter JL et al.

Human Mutation, 2003

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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."