Have questions? Visit https://www.reddit.com/r/SNPedia

rs80359341

From SNPedia

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


Make rs80359341(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319275
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359341
ebirs80359341
HLIrs80359341
Exacrs80359341
Varsomers80359341
Maprs80359341
PheGenIrs80359341
hapmaprs80359341
1000 genomesrs80359341
hgdprs80359341
ensemblrs80359341
gopubmedrs80359341
geneviewrs80359341
scholarrs80359341
googlers80359341
pharmgkbrs80359341
gwascentralrs80359341
openSNPrs80359341
23andMers80359341
23andMe allrs80359341
SNP Nexus

SNPshotrs80359341
SNPdbers80359341
MSV3drs80359341
GWAS Ctlgrs80359341
Max Magnitude6
rs80359341, also known as 494delC, c.266_266delC and p.Pro89Argfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359341(;)
Alt rs80359341(;)
Reference rs80359341(C;C)
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.32893412delC
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044035.2, RCV000113337.1,