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rs80359803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359803(A;A)
Make rs80359803(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376791
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359803
ebirs80359803
HLIrs80359803
Exacrs80359803
Varsomers80359803
Maprs80359803
PheGenIrs80359803
hapmaprs80359803
1000 genomesrs80359803
hgdprs80359803
ensemblrs80359803
gopubmedrs80359803
geneviewrs80359803
scholarrs80359803
googlers80359803
pharmgkbrs80359803
gwascentralrs80359803
openSNPrs80359803
23andMers80359803
23andMe allrs80359803
SNP Nexus

SNPshotrs80359803
SNPdbers80359803
MSV3drs80359803
GWAS Ctlgrs80359803
Max Magnitude0
ClinVar
Risk rs80359803(A;A)
Alt rs80359803(A;A)
Reference rs80359803(G;G)
Significance Pathogenic
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.32950928G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045618.2, RCV000077451.3, RCV000131042.2,