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rs80359625

From SNPedia

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


Make rs80359625(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341164
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359625
ebirs80359625
HLIrs80359625
Exacrs80359625
Varsomers80359625
Maprs80359625
PheGenIrs80359625
hapmaprs80359625
1000 genomesrs80359625
hgdprs80359625
ensemblrs80359625
gopubmedrs80359625
geneviewrs80359625
scholarrs80359625
googlers80359625
pharmgkbrs80359625
gwascentralrs80359625
openSNPrs80359625
23andMers80359625
23andMe allrs80359625
SNP Nexus

SNPshotrs80359625
SNPdbers80359625
MSV3drs80359625
GWAS Ctlgrs80359625
Max Magnitude6
rs80359625, also known as 7037delG, c.6809_6809delG and p.Gly2270Glufs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359625(;)
Alt rs80359625(;)
Reference rs80359625(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.32915301delG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045056.2, RCV000113648.1,