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rs80359205

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs80359205(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394749
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359205
ebirs80359205
HLIrs80359205
Exacrs80359205
Varsomers80359205
Maprs80359205
PheGenIrs80359205
hapmaprs80359205
1000 genomesrs80359205
hgdprs80359205
ensemblrs80359205
gopubmedrs80359205
geneviewrs80359205
scholarrs80359205
googlers80359205
pharmgkbrs80359205
gwascentralrs80359205
openSNPrs80359205
23andMers80359205
23andMe allrs80359205
SNP Nexus

SNPshotrs80359205
SNPdbers80359205
MSV3drs80359205
GWAS Ctlgrs80359205
Max Magnitude6
rs80359205, also known as W3106X, c.9317G>A and p.Trp3106Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359205(A;A)
Alt rs80359205(A;A)
Reference rs80359205(G;G)
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.32968886G>A
CLNSRC ClinVar
CLNACC RCV000045792.2, RCV000114090.1,