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rs80359251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359251(A;A)
Make rs80359251(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398438
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359251
ebirs80359251
HLIrs80359251
Exacrs80359251
Varsomers80359251
Maprs80359251
PheGenIrs80359251
hapmaprs80359251
1000 genomesrs80359251
hgdprs80359251
ensemblrs80359251
gopubmedrs80359251
geneviewrs80359251
scholarrs80359251
googlers80359251
pharmgkbrs80359251
gwascentralrs80359251
openSNPrs80359251
23andMers80359251
23andMe allrs80359251
SNP Nexus

SNPshotrs80359251
SNPdbers80359251
MSV3drs80359251
GWAS Ctlgrs80359251
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs80359251(A,T;A,T)
Alt rs80359251(A,T;A,T)
Reference rs80359251(G;G)
Significance Other
Disease Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32972575G>A; NC_000013.10:g.32972575G>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000112824.1, RCV000120378.2, RCV000130750.2, RCV000195387.3, RCV000045917.2, RCV000112825.1,