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rs80359032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359032(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363198
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359032
ebirs80359032
HLIrs80359032
Exacrs80359032
Varsomers80359032
Maprs80359032
PheGenIrs80359032
hapmaprs80359032
1000 genomesrs80359032
hgdprs80359032
ensemblrs80359032
gopubmedrs80359032
geneviewrs80359032
scholarrs80359032
googlers80359032
pharmgkbrs80359032
gwascentralrs80359032
openSNPrs80359032
23andMers80359032
23andMe allrs80359032
SNP Nexus

SNPshotrs80359032
SNPdbers80359032
MSV3drs80359032
GWAS Ctlgrs80359032
Max Magnitude6
rs80359032, also known as R2666X, c.7996A>T and p.Arg2666Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359032(T;T)
Alt rs80359032(T;T)
Reference rs80359032(A;A)
Significance Pathogenic
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.32937335A>T
CLNSRC ClinVar
CLNACC RCV000045379.2, RCV000113853.1,