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rs80359142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar
Make rs80359142(G;G)
Make rs80359142(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379477
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359142
dbSNP (old)rs80359142
ClinGenrs80359142
ebirs80359142
HLIrs80359142
Exacrs80359142
Varsomers80359142
Maprs80359142
PheGenIrs80359142
Biobankrs80359142
1000 genomesrs80359142
hgdprs80359142
ensemblrs80359142
gopubmedrs80359142
geneviewrs80359142
scholarrs80359142
googlers80359142
pharmgkbrs80359142
gwascentralrs80359142
openSNPrs80359142
23andMers80359142
23andMe allrs80359142
SNP Nexus

SNPshotrs80359142
SNPdbers80359142
MSV3drs80359142
GWAS Ctlgrs80359142
Max Magnitude6
ClinVar
Risk rs80359142(A;A) rs80359142(G;G)
Alt rs80359142(A;A) rs80359142(G;G)
Reference Rs80359142(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953614T>A; NC_000013.10:g.32953614T>G
CLNSRC ClinVar
CLNACC RCV000256493.2, RCV000429396.1, RCV000045654.4, RCV000114014.1, RCV000212282.1, RCV000215767.1,