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SNP information rs28897706

RS28897706

Normal allele: CC

Polymorphism rs28897706 is related to topics like this:

BRCA gene

BRCA stands for "BReast CAncer gene" and refers to two distinct genes, BRCA1 and BRCA2, which have...


Research and publications:

  10399947   Germline brca2 sequence variants in patients with ocular melanoma.

  10728701   BRCA1 and BRCA2 have a limited role in familial prostate cancer.

  11106241   BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers.

  11304778   Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinic.

  12474142   Two percent of men with early-onset prostate cancer harbor germline mutations in the BRCA2 gene.

  18284688   Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: results from a population-based study of young breast cancer patients.

  18724707   Computational and structural investigation of deleterious functional SNPs in breast cancer BRCA2 gene.

  18824701   Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance.

  19941162   High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays.

  21520273   Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.

  21702907   A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.

  21952622   BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients.

  21990134   A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).

  22729890   A 24-color metaphase-based radiation assay discriminates heterozygous BRCA2 mutation carriers from controls by chromosomal radiosensitivity.

  23231788   Variants of uncertain significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counselling.

  24033266   A systematic approach to assessing the clinical significance of genetic variants.

  24728327   Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.

  25637381   Actionable exomic incidental findings in 6503 participants: challenges of variant classification.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  24055113   Actionable, pathogenic incidental findings in the exomes of 1000 participants.

DNA diet

The DNA Diet report is tailored to assist with weight management by offering personalized diet and...

Keto genetics

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Low calorie diet genetic

Dieters can determine which diet would result in more weight loss by undergoing a genetic test,...

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