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SNP information rs28897710

RS28897710

Normal allele: AA

Polymorphism rs28897710 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:

  12215251   Characterization of common BRCA1 and BRCA2 variants.

  12845657   Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: a population-based study.

  16683254   A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.

  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.

  18414213   ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

  19471317   Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.

  20104584   Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

  20383589   Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.

  21232165   The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population.

  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.

  22366370   Three novel BRCA1/BRCA2 mutations in breast/ovarian cancer families in Croatia.

  22703879   Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

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

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

  24171766   Common low-penetrance risk variants associated with breast cancer in Polish women.

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

  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.

DNA diet

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

Keto genetics

The KD, a diet low in carbohydrates and high in fat and protein, has been shown to effectively...

Low calorie diet genetic

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

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