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rs80359061

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359061(A;A)
Make rs80359061(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363364
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359061
ebirs80359061
HLIrs80359061
Exacrs80359061
Varsomers80359061
Maprs80359061
PheGenIrs80359061
hapmaprs80359061
1000 genomesrs80359061
hgdprs80359061
ensemblrs80359061
gopubmedrs80359061
geneviewrs80359061
scholarrs80359061
googlers80359061
pharmgkbrs80359061
gwascentralrs80359061
openSNPrs80359061
23andMers80359061
23andMe allrs80359061
SNP Nexus

SNPshotrs80359061
SNPdbers80359061
MSV3drs80359061
GWAS Ctlgrs80359061
Max Magnitude0
ClinVar
Risk rs80359061(A,G;A,G)
Alt rs80359061(A,G;A,G)
Reference rs80359061(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32937501T>A; NC_000013.10:g.32937501T>G
CLNSRC ClinVar
CLNACC RCV000045433.2, RCV000113878.1, RCV000223648.1, RCV000045434.2,