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SNP information rs1801426

RS1801426

Normal allele: AA

Polymorphism rs1801426 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:

  8640236   Low incidence of BRCA2 mutations in breast carcinoma and other cancers.

  9150152   A low proportion of BRCA2 mutations in Finnish breast cancer families.

  9971877   Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations.

  11389159   BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

  12453858   BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counseling.

  14647438   Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer.

  15317758   Common variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort.

  17341484   Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility.

  21356067   Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals.

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

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

  23469205   Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.

  23961350   BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin.

  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.

  24884479   Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.

  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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