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rs80359075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80359075(C;T)
Make rs80359075(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370420
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359075
ebirs80359075
HLIrs80359075
Exacrs80359075
Varsomers80359075
Maprs80359075
PheGenIrs80359075
hapmaprs80359075
1000 genomesrs80359075
hgdprs80359075
ensemblrs80359075
gopubmedrs80359075
geneviewrs80359075
scholarrs80359075
googlers80359075
pharmgkbrs80359075
gwascentralrs80359075
openSNPrs80359075
23andMers80359075
23andMe allrs80359075
SNP Nexus

SNPshotrs80359075
SNPdbers80359075
MSV3drs80359075
GWAS Ctlgrs80359075
Max Magnitude0
ClinVar
Risk rs80359075(T;T)
Alt rs80359075(T;T)
Reference rs80359075(C;C)
Significance Untested
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944557C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031738.4, RCV000045487.4, RCV000131691.2,