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rs80359142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359142(G;G)
Make rs80359142(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379477
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359142
ebirs80359142
HLIrs80359142
Exacrs80359142
Varsomers80359142
Maprs80359142
PheGenIrs80359142
hapmaprs80359142
1000 genomesrs80359142
hgdprs80359142
ensemblrs80359142
gopubmedrs80359142
geneviewrs80359142
scholarrs80359142
googlers80359142
pharmgkbrs80359142
gwascentralrs80359142
openSNPrs80359142
23andMers80359142
23andMe allrs80359142
SNP Nexus

SNPshotrs80359142
SNPdbers80359142
MSV3drs80359142
GWAS Ctlgrs80359142
Max Magnitude0
ClinVar
Risk rs80359142(G;G)
Alt rs80359142(G;G)
Reference rs80359142(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32953614T>G
CLNSRC ClinVar
CLNACC RCV000045654.4, RCV000114014.1, RCV000212282.1, RCV000215767.1,