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SNP information rs4973768

RS4973768

Normal allele: CC

Polymorphism rs4973768 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:

  19330027   Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

  19519208   Polygenic susceptibility to breast cancer: current state-of-the-art.

  19639606   Correcting the “winner's curse” in odds ratios based on genome-wide association results for major complex human diseases.

  20095854   Novel breast cancer risk alleles and interaction with ionizing radiation among U.S. radiologic technologists.

  20146796   Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.

  20418484   Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

  20453838   Genome-wide association study identifies five new breast cancer susceptibility loci.

  20505153   A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.

  20585100   Genome-wide association studies of cancer.

  20699374   Evaluation of breast cancer susceptibility loci in Chinese women.

  20718042   Pooled versus individual genotyping in a breast cancer genome-wide association study.

  20957429   Discriminatory accuracy and potential clinical utility of genomic profiling for breast cancer risk in BRCA-negative women.

  21102626   Caution in generalizing known genetic risk markers for breast cancer across all ethnic/racial populations.

  21118973   Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

  21194473   Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study.

  21219822   [Recent progress in genetic variants associated with cancer and their implications in diagnostics development].

  21415360   Common genetic variants associated with breast cancer in Korean women and differential susceptibility according to intrinsic subtype.

  21445572   Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies.

  21468051   Polygenic susceptibility to prostate and breast cancer: implications for personalised screening.

  21514219   Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence

  21596841   Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.

  21639959   Annual conference on hereditary cancers 2009 szczecin, poland. 10-11 december 2009. Abstracts.

  21791674   Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium.

  21795501   Replication of GWAS breast cancer susceptibility loci in the Women's Health Initiative African American SHARe Study.

  21844186   Common breast cancer susceptibility loci are associated with triple-negative breast cancer.

  21852243   Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans.

  21869864   An integrative genomics approach to biomarker discovery in breast cancer.

  21949660   Genetic variants at chromosomes 2q35, 5p12, 6q25.1, 10q26.13, and 16q12.1 influence the risk of breast cancer in men.

  22028405   Estimating causal effects of genetic risk variants for breast cancer using marker data from bilateral and familial cases.

  22053997   Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

  22160591   A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population.

  22269215   Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women.

  22287734   Evaluation of breast cancer susceptibility loci on 2q35, 3p24, 17q23 and FGFR2 genes in Taiwanese women with breast cancer.

  22314178   Breast cancer risk prediction and individualised screening based on common genetic variation and breast density measurement.

  22357627   Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry.

  22452962   A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.

  22454379   Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk.

  22532573   The role of genetic breast cancer susceptibility variants as prognostic factors.

  22606281   Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways.

  22747683   Genetic variants associated with breast size also influence breast cancer risk.

  22972951   Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status.

  23117855   The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case-control study and a meta-analysis.

  23136140   Genetic susceptibility loci for subtypes of breast cancer in an African American population.

  23221726   Gene-environment interactions for breast cancer risk among Chinese women: a report from the Shanghai Breast Cancer Genetics Study.

  23474973   Incremental impact of breast cancer SNP panel on risk classification in a screening population of white and African American women.

  23535825   Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls.

  23544014   Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors.

  23593120   Evaluating genome-wide association study-identified breast cancer risk variants in African-American women.

  23635555   The relationship between eight GWAS-identified single-nucleotide polymorphisms and primary breast cancer outcomes.

  23650637   Deconvoluting complex tissues for expression quantitative trait locus-based analyses.

  23717390   Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm.

  23893088   The associations between a polygenic score, reproductive and menstrual risk factors and breast cancer risk.

  24025454   Hereditary breast cancer: ever more pieces to the polygenic puzzle.

  24218030   Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.

  24265035   Risk of GWAS-identified genetic variants for breast cancer in a Chinese population: a multiple interaction analysis.

  24266904   Breast cancer prediction using genome wide single nucleotide polymorphism data.

  24359602   Common breast cancer risk variants in the post-COGS era: a comprehensive review.

  24373701   Breast cancer susceptibility loci in association with age at menarche, age at natural menopause and the reproductive lifespan.

  24510657   Evaluating 17 breast cancer susceptibility loci in the Nashville breast health study.

  24771903   Breast Cancer Risk - From Genetics to Molecular Understanding of Pathogenesis.

  24792587   Reproductive windows, genetic loci, and breast cancer risk.

  24895409   Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women.

  24941967   Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population.

  24943594   Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.

  25027274   Testing calibration of risk models at extremes of disease risk.

  25057183   A robust association test for detecting genetic variants with heterogeneous effects.

  25198130   Integrative genomic analysis identifies that SERPINA6-rs1998056 regulated by FOXA/ERα is associated with female hepatocellular carcinoma.

  25253900   Breast Cancer Risk - Genes, Environment and Clinics.

  25255808   Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.

  25526632   A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis.

  25567532   The use of the Gail model, body mass index and SNPs to predict breast cancer among women with abnormal (BI-RADS 4) mammograms.

  25611573   Association of breast cancer risk loci with breast cancer survival.

  25881232   Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography.

  26070784   Genetic risk variants associated with in situ breast cancer.

  26175953   FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population.

  26510858   Patients with a High Polygenic Risk of Breast Cancer do not have An Increased Risk of Radiotherapy Toxicity.

  26884359   Genetic predisposition to ductal carcinoma in situ of the breast.

  27079684   Genome-wide association studies and epigenome-wide association studies go together in cancer control.

  27392074   The Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case-Control Study.

  27424552   Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.

  27438779   Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families.

  28098224   Association of Genome-Wide Association Study (GWAS) Identified SNPs and Risk of Breast Cancer in an Indian Population.

  28178648   Polymorphisms of ESR1, UGT1A1, HCN1, MAP3K1 and CYP2B6 are associated with the prognosis of hormone receptor-positive early breast cancer.

  28757652   Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.

  29029469   Genetic and environmental factors and serum hormones, and risk of estrogen receptor-positive breast cancer in pre- and postmenopausal Japanese women.

  29382703   Common Genetic Variation and Breast Cancer Risk-Past, Present, and Future.

  31125336   Evaluation of significant genome-wide association studies risk - SNPs in young breast cancer patients.

  32269954   Copy number alternations of the 17q23-rs6504950 locus are associated with advanced breast cancers in Taiwanese women.

  32366738   Low-penetrance susceptibility variants and postmenopausal oestrogen receptor positive breast cancer.

  32823908   Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa.

  32894086   MassARRAY-based single nucleotide polymorphism analysis in breast cancer of north Indian population.

  34359697   A Personal Breast Cancer Risk Stratification Model Using Common Variants and Environmental Risk Factors in Japanese Females.

  35395775   Development and validation of polygenic risk scores for prediction of breast cancer and breast cancer subtypes in Chinese women.

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