Rs3803662

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is asnp
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dbSNPrs3803662
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hgdprs3803662
ensemblrs3803662
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pharmgkbrs3803662
hgvbaseg2prs3803662
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23andMers3803662
SNP Nexus

GeneLOC643714
Chromosome16
Orientationminus
Position51143842
GenotypeEffect
rs3803662(C;C)normal
rs3803662(C;T)?
rs3803662(T;T)1.6x increased risk for breast cancer


Genotypes Magnitude Summary
Rs3803662(C;C) 00 normal
Rs3803662(C;T) ?
Rs3803662(G;G) 00
Rs3803662(T;T) 1.6x increased risk for breast cancer

rs3803662, a SNP associated with the TNRC9 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]

[PMID 17529974] rs3803662(T;T) have a 1.64-fold greater risk of estrogen receptor-positive tumors

In a study of 1,267 breast cancer patients, rs3803662 heterozygote carriers and minor allele homozygote carriers were more likely to be diagnosed before the age of 60 years (p = 0.025) relative to major allele homozygote carriers.[PMID 17997823]

[PMID 18437204] breast cancer

  • rs2981582, rs3803662, and rs889312) showed weak but significant associations with ER-negative disease, the strongest association being for rs3803662 in TNRC9 (1.14 (1.09-1.21))

[PMID 19005751] rs3803662 confirmed in 988 sporadic breast cancer cases and 1,016 controls from the West of Ireland to be associated with increased risk (odds ratio 1.15, p(allelic) = 5.1 x 10e-2) for breast cancer

? (C;C) (C;T) (T;T)
GWAS
SNP rs3803662
PubMedID [PMID 17529974]
Condition Breast cancer
Gene TNRC9
Risk Allele T
pValue 6.00E-019
OR 1.28
95% CI 1.21-1.35


GWAS snp
PMID [PMID 19330030]
Trait Breast cancer
Title A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
Risk Allele T
P-val 1E-9
Odds Ratio
Related to BREAST CANCER according to omim 114480. See also


Related to BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1 according to omim 604370. See also


Related to TOX HIGH MOBILITY GROUP BOX FAMILY MEMBER 3; TOX3 according to omim 611416. See also


PharmGKBPA161925624
Name
AnnotationThis variant is significantly associated with risk for breast cancer from multiple large scale genome wide association studies. Carriers of the T allele had a 1.64-fold greater risk of estrogen receptor-positive breast cancer and were more likely to be diagnosed before the age of 60 years.
Gene-
Featue
EvidencePubMed ID:17529967; PubMed ID:17529974; PubMed ID:17997823
Drugs
DiseasesBreast Neoplasms
Curation LevelCurated