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rs80359147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359147(A;G)
Make rs80359147(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379758
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359147
ebirs80359147
HLIrs80359147
Exacrs80359147
Varsomers80359147
Maprs80359147
PheGenIrs80359147
hapmaprs80359147
1000 genomesrs80359147
hgdprs80359147
ensemblrs80359147
gopubmedrs80359147
geneviewrs80359147
scholarrs80359147
googlers80359147
pharmgkbrs80359147
gwascentralrs80359147
openSNPrs80359147
23andMers80359147
23andMe allrs80359147
SNP Nexus

SNPshotrs80359147
SNPdbers80359147
MSV3drs80359147
GWAS Ctlgrs80359147
Max Magnitude0
ClinVar
Risk rs80359147(G;G)
Alt rs80359147(G;G)
Reference rs80359147(A;A)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953895A>G
CLNSRC ClinVar
CLNACC RCV000045674.2, RCV000114024.1,