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rs80359764

From SNPedia

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


Make rs80359764(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394887
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359764
ebirs80359764
HLIrs80359764
Exacrs80359764
Varsomers80359764
Maprs80359764
PheGenIrs80359764
hapmaprs80359764
1000 genomesrs80359764
hgdprs80359764
ensemblrs80359764
gopubmedrs80359764
geneviewrs80359764
scholarrs80359764
googlers80359764
pharmgkbrs80359764
gwascentralrs80359764
openSNPrs80359764
23andMers80359764
23andMe allrs80359764
SNP Nexus

SNPshotrs80359764
SNPdbers80359764
MSV3drs80359764
GWAS Ctlgrs80359764
Max Magnitude6
rs80359764, also known as 9683delAG, c.9455_9456delAG and p.Glu3152Glyfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359764(;)
Alt rs80359764(;)
Reference rs80359764(AG;AG)
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.32969024_32969025delAG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045824.2, RCV000083160.3,