Rs3817198

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dbSNPrs3817198
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hgdprs3817198
ensemblrs3817198
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scholarrs3817198
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pharmgkbrs3817198
hgvbaseg2prs3817198
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23andMers3817198
SNP Nexus

GeneLSP1
Chromosome11
Orientationplus
Position1865581
GenotypeEffect
rs3817198(C;C)*?
rs3817198(C;T)*?
rs3817198(T;T)*?


rs3817198, a SNP associated with the LSP1 gene, was one of the four strongest associating SNPs found in a genome-wide association study of over 4,000 breast cancer samples.[PMID 17529967]
? (C;C) (C;T) (T;T)
GWAS
SNP rs3817198
PubMedID [PMID 17529967]
Condition Breast cancer
Gene LSP1
Risk Allele T
pValue 3.00E-009
OR 1.07
95% CI 1.04-1.11


Related to BREAST CANCER according to omim 114480. See also


Related to LYMPHOCYTE-SPECIFIC PROTEIN; LSP1 according to omim 153432. See also


[PMID 19656774] Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

PharmGKBPA162356624
Name
AnnotationGWAS Results: Genome-wide association study identifies novel breast cancer susceptibility loci (Initial Sample Size: 390 cases, 364 controls; Replication Sample Size: 26,646 cases, 24,889 controls; Risk Allele: rs3817198-T).
GeneLSP1
Featue
EvidencePubMed ID:17529967; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesBreast Neoplasms
Curation LevelNon-Curated