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rs80358978

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358978(A;A)
Make rs80358978(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356514
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358978
ebirs80358978
HLIrs80358978
Exacrs80358978
Varsomers80358978
Maprs80358978
PheGenIrs80358978
hapmaprs80358978
1000 genomesrs80358978
hgdprs80358978
ensemblrs80358978
gopubmedrs80358978
geneviewrs80358978
scholarrs80358978
googlers80358978
pharmgkbrs80358978
gwascentralrs80358978
openSNPrs80358978
23andMers80358978
23andMe allrs80358978
SNP Nexus

SNPshotrs80358978
SNPdbers80358978
MSV3drs80358978
GWAS Ctlgrs80358978
Max Magnitude0

[PMID 24470074OA-icon.png] Rare coding variants and breast cancer risk: Evaluation of susceptibility loci identified in genome-wide association studies

ClinVar
Risk rs80358978(A;A)
Alt rs80358978(A;A)
Reference rs80358978(G;G)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32930651G>A
CLNSRC ClinVar
CLNACC RCV000045236.4, RCV000077404.4, RCV000120359.1, RCV000164682.1, RCV000203651.1,