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rs80359067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80359067(C;T)
Make rs80359067(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363391
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359067
ebirs80359067
HLIrs80359067
Exacrs80359067
Varsomers80359067
Maprs80359067
PheGenIrs80359067
hapmaprs80359067
1000 genomesrs80359067
hgdprs80359067
ensemblrs80359067
gopubmedrs80359067
geneviewrs80359067
scholarrs80359067
googlers80359067
pharmgkbrs80359067
gwascentralrs80359067
openSNPrs80359067
23andMers80359067
23andMe allrs80359067
SNP Nexus

SNPshotrs80359067
SNPdbers80359067
MSV3drs80359067
GWAS Ctlgrs80359067
Max Magnitude0
ClinVar
Risk rs80359067(T;T)
Alt rs80359067(T;T)
Reference Rs80359067(C;C)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937528C>T
CLNSRC ClinVar
CLNACC RCV000045446.2, RCV000113887.1,