SNP information rs1562430

Research and publications:

  19330030   A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

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

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

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

  21779458   Chromosome 8q24-Associated Cancers and MYC.

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

  22275265   Common genetic variants in the 8q24 region and risk of papillary thyroid cancer.

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

  22558003   The 8q24 gene desert: an oasis of non-coding transcriptional activity.

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

  22806168   A multistage genetic association study identifies breast cancer risk loci at 10q25 and 16q24.

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

  23486537   Comparison of genetic variation of breast cancer susceptibility genes in Chinese and German populations.

  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.

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

  24875630   Validation of six genetic determinants of susceptibility to estrogen-induced mammary cancer in the rat and assessment of their relevance to breast cancer risk in humans.

  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.

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

  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.

  25302443   Genetic variant in 8q24 is associated with prognosis for gastric cancer in a Chinese population.

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

  26070784   Genetic risk variants associated with in situ breast cancer.

  26248686   Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: results from a multicenter study in Italy.

  27022606   Associations of Genetic Variants at Nongenic Susceptibility Loci with Breast Cancer Risk and Heterogeneity by Tumor Subtype in Southern Han Chinese Women.

  27814745   Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities.

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

  30285756   Subtype-specific associations between breast cancer risk polymorphisms and the survival of early-stage breast cancer.

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

  32117633   Long non-coding RNA polymorphisms on 8q24 are associated with the prognosis of gastric cancer in a Chinese population.

  32875717   Long non-coding RNA CASC8 polymorphisms are associated with the risk of esophageal cancer in a Chinese population.