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rs80359041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359041(A;G)
Make rs80359041(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363238
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359041
ebirs80359041
HLIrs80359041
Exacrs80359041
Varsomers80359041
Maprs80359041
PheGenIrs80359041
hapmaprs80359041
1000 genomesrs80359041
hgdprs80359041
ensemblrs80359041
gopubmedrs80359041
geneviewrs80359041
scholarrs80359041
googlers80359041
pharmgkbrs80359041
gwascentralrs80359041
openSNPrs80359041
23andMers80359041
23andMe allrs80359041
SNP Nexus

SNPshotrs80359041
SNPdbers80359041
MSV3drs80359041
GWAS Ctlgrs80359041
Max Magnitude0
ClinVar
Risk rs80359041(G;G)
Alt rs80359041(G;G)
Reference rs80359041(A;A)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32937375A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045397.2, RCV000113859.1, RCV000131797.2,