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rs80359071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359071(A;A)
Make rs80359071(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363445
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359071
ebirs80359071
HLIrs80359071
Exacrs80359071
Varsomers80359071
Maprs80359071
PheGenIrs80359071
hapmaprs80359071
1000 genomesrs80359071
hgdprs80359071
ensemblrs80359071
gopubmedrs80359071
geneviewrs80359071
scholarrs80359071
googlers80359071
pharmgkbrs80359071
gwascentralrs80359071
openSNPrs80359071
23andMers80359071
23andMe allrs80359071
SNP Nexus

SNPshotrs80359071
SNPdbers80359071
MSV3drs80359071
GWAS Ctlgrs80359071
Max Magnitude0
ClinVar
Risk rs80359071(A;A)
Alt rs80359071(A;A)
Reference rs80359071(G;G)
Significance Pathogenic
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.32937582G>A
CLNSRC ClinVar
CLNACC RCV000045460.2, RCV000113895.2, RCV000216216.1,