
NCBI . NLM . NIH . GOV {
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Title[redir]:
Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study - PMC
Description:
Two single nucleotide polymorphisms (SNPs), rs4415084, and rs10941679 on chromosome 5p12 were associated with risk of breast cancer in a recent genome-wide association study (GWAS) of women of European ancestry. Both SNPs are located in a large ...
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Keywords {🔍}
cancer, breast, doi, snps, study, cases, risk, association, region, boston, pubmed, google, scholar, health, snp, controls, pmc, block, women, samples, gwas, university, usa, variants, european, article, admixture, population, center, populations, bwhs, free, table, genet, tumors, identified, genotyping, analysis, black, womens, results, ceu, epidemiology, nlm, national, genetic, chromosome, located, tagging, observed,
Topics {✒️}
org/sections/science/projects/broad/ncrr-center-genotyping-analysis genome-wide association scans cochran–armitage trend test pmc beta search high-density admixture map genome-wide association level multi-ethnic cohort study mouthwash-swish saliva samples case–control status labels population-based linkage analyses nested case–control study nested-case control study high-risk allele frequency nigerian case-control study broad institute center large high-ld region publisher site pdf breast cancer identifies license information pmcid including european admixture org/haploview/haploview gene expression profile methods study population percent european admixture final edited form potential confounding factors ancestral informative markers high-risk alleles national cancer institute de bakker pi body mass index 1007/s10549-010-0775-5 genetic variants entire ld block european admixture proportion percent european ancestry logistic regression analysis united states government single nucleotide polymorphisms united states completed mouthwash-swish method [11] institutional review boards hardy–weinberg equilibrium additive genetic model lower panels show grant u54 rr020278 brca2 mutation carriers med womens assoc minor allele frequency discrete ld blocks ceu ld block
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