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rs80359765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;AG) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359765(-;-)
Make rs80359765(AG;AG)
ReferenceGRCh38 38.1/142
Chromosome13
Position32394888
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359765
ebirs80359765
HLIrs80359765
Exacrs80359765
Varsomers80359765
Maprs80359765
PheGenIrs80359765
hapmaprs80359765
1000 genomesrs80359765
hgdprs80359765
ensemblrs80359765
gopubmedrs80359765
geneviewrs80359765
scholarrs80359765
googlers80359765
pharmgkbrs80359765
gwascentralrs80359765
openSNPrs80359765
23andMers80359765
23andMe allrs80359765
SNP Nexus

SNPshotrs80359765
SNPdbers80359765
MSV3drs80359765
GWAS Ctlgrs80359765
Max Magnitude6
rs80359765, also known as 9684insAG, c.9456_9457insAG and p.Glu3152_Gly3153?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359765(AG;AG)
Alt rs80359765(AG;AG)
Reference rs80359765(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32969024_32969025dupAG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000114110.1,