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rs80359603

From SNPedia

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


Make rs80359603(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340908
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359603
ebirs80359603
HLIrs80359603
Exacrs80359603
Varsomers80359603
Maprs80359603
PheGenIrs80359603
hapmaprs80359603
1000 genomesrs80359603
hgdprs80359603
ensemblrs80359603
gopubmedrs80359603
geneviewrs80359603
scholarrs80359603
googlers80359603
pharmgkbrs80359603
gwascentralrs80359603
openSNPrs80359603
23andMers80359603
23andMe allrs80359603
SNP Nexus

SNPshotrs80359603
SNPdbers80359603
MSV3drs80359603
GWAS Ctlgrs80359603
Max Magnitude6
rs80359603, also known as 6781delG, c.6553_6553delG and p.Ala2185Leufs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359603(;)
Alt rs80359603(;)
Reference rs80359603(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.32915045delG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044983.2, RCV000113609.1,