Research Notes on Rs3817198
Variations in the DNA sequences of humans -- called single nucleotide polymorphism (SNPs) -- can affect how an individual develops diseases and responds to pathogens, chemicals, drugs, vaccines, and other agents. SNP rs3817198 is one of the four SNPs found to be most strongly associated with breast cancer.
Top Resources on Rs3817198
- SNPedia: rs3817198
- Breast Cancer Research: Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases
- Proceedings of the National Academy of Sciences: Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33
- National Center for Genome Resources: Genome-Wise Association Studies: Progress in Identifying Genetic Biomarkers in Common, Complex Diseases
- ENH Research Institute: In Search of Breast Cancer Culprits: Suspecting the Suspected and the Unsuspected
- National Cancer Research Institute: Association of Recently Identified Common Low Penetrance Breast Cancer Susceptibility Alleles with Molecular Pathological Subtypes of Disease
- Whitehead Institute for Biomedical Research: Deciphering the Human Genome and the MS Project
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About this WisdomCard
- Contributor: Nicole Kinsey
- Reviewer: ASandhu
- Supervised by: The OrganizedWisdom Physician Review Team
- Last update: Aug. 12, 2008
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