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

rs80359334

From SNPedia

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


Make rs80359334(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336919
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359334
ebirs80359334
HLIrs80359334
Exacrs80359334
Varsomers80359334
Maprs80359334
PheGenIrs80359334
hapmaprs80359334
1000 genomesrs80359334
hgdprs80359334
ensemblrs80359334
gopubmedrs80359334
geneviewrs80359334
scholarrs80359334
googlers80359334
pharmgkbrs80359334
gwascentralrs80359334
openSNPrs80359334
23andMers80359334
23andMe allrs80359334
SNP Nexus

SNPshotrs80359334
SNPdbers80359334
MSV3drs80359334
GWAS Ctlgrs80359334
Max Magnitude6
rs80359334, also known as 2792delCA, c.2564_2565delCA and p.Thr855Lysfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359334(;)
Alt rs80359334(;)
Reference rs80359334(AC;AC)
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.32911056_32911057delCA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044017.2, RCV000113062.1,