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rs80359079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359079(C;C)
Make rs80359079(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370432
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359079
ebirs80359079
HLIrs80359079
Exacrs80359079
Varsomers80359079
Maprs80359079
PheGenIrs80359079
hapmaprs80359079
1000 genomesrs80359079
hgdprs80359079
ensemblrs80359079
gopubmedrs80359079
geneviewrs80359079
scholarrs80359079
googlers80359079
pharmgkbrs80359079
gwascentralrs80359079
openSNPrs80359079
23andMers80359079
23andMe allrs80359079
SNP Nexus

SNPshotrs80359079
SNPdbers80359079
MSV3drs80359079
GWAS Ctlgrs80359079
Max Magnitude0
ClinVar
Risk rs80359079(C,G;C,G)
Alt rs80359079(C,G;C,G)
Reference rs80359079(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.32944569T>C
CLNSRC ClinVar
CLNACC RCV000045493.2, RCV000113915.1, RCV000219719.1,