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SNP information rs28897683

RS28897683

Normal allele: GG

Polymorphism rs28897683 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:

  7837387   A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening.

  9792861   Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.

  10635334   Genetic analysis of BRCA1 function in a defined tumor cell line.

  10882858   Incidence of BRCA1/2 germ line alterations in a high risk cohort participating in a phase II chemoprevention trial.

  11802209   Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population.

  16267036   Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.

  16518693   Natural selection and mammalian BRCA1 sequences: elucidating functionally important sites relevant to breast cancer susceptibility in humans.

  16905680   Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer.

  18375895   Clinical classification of BRCA1 and BRCA2 DNA sequence variants: the value of cytokeratin profiles and evolutionary analysis--a report from the kConFab Investigators.

  18446624   Histopathological features of familial breast cancer BRCAX in the kConFab resource.

  19619314   A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population.

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

  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.

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

  23867111   A high-throughput functional complementation assay for classification of BRCA1 missense variants.

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

  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.

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