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rs80358891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80358891(G;G)
Make rs80358891(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32329474
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358891
ebirs80358891
HLIrs80358891
Exacrs80358891
Varsomers80358891
Maprs80358891
PheGenIrs80358891
hapmaprs80358891
1000 genomesrs80358891
hgdprs80358891
ensemblrs80358891
gopubmedrs80358891
geneviewrs80358891
scholarrs80358891
googlers80358891
pharmgkbrs80358891
gwascentralrs80358891
openSNPrs80358891
23andMers80358891
23andMe allrs80358891
SNP Nexus

SNPshotrs80358891
SNPdbers80358891
MSV3drs80358891
GWAS Ctlgrs80358891
Max Magnitude0
ClinVar
Risk rs80358891(G;G)
Alt rs80358891(G;G)
Reference rs80358891(T;T)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32903611T>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031640.5, RCV000045003.2, RCV000132202.2,