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rs3737559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in complete genomics
Make rs3737559(A;A)
Make rs3737559(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082287
GeneBRCA1
is asnp
is mentioned by
dbSNPrs3737559
ebirs3737559
HLIrs3737559
Exacrs3737559
Varsomers3737559
Maprs3737559
PheGenIrs3737559
hapmaprs3737559
1000 genomesrs3737559
hgdprs3737559
ensemblrs3737559
gopubmedrs3737559
geneviewrs3737559
scholarrs3737559
googlers3737559
pharmgkbrs3737559
gwascentralrs3737559
openSNPrs3737559
23andMers3737559
23andMe allrs3737559
SNP Nexus

SNPshotrs3737559
SNPdbers3737559
MSV3drs3737559
GWAS Ctlgrs3737559
GMAF0.06336
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 21598251] Genetic polymorphisms in AURKA and BRCA1 are associated with breast cancer susceptibility in a Chinese Han population


[PMID 15743496OA-icon.png] Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer.


[PMID 17428325OA-icon.png] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.


[PMID 18701471OA-icon.png] Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.


[PMID 19276285OA-icon.png] Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.


[PMID 20039378OA-icon.png] Estimation of genotype relative risks from pedigree data by retrospective likelihoods.


ClinVar
Risk rs3737559(A;A)
Alt rs3737559(A;A)
Reference rs3737559(G;G)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41234304C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000112322.2,



[PMID 25463638] Association of genetic polymorphisms in AURKA, BRCA1, CCNE1 and CDK2 with the risk of endometrial carcinoma and clinicopathological parameters among Chinese Han women