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rs80359726

From SNPedia

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


Make rs80359726(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376750
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359726
ebirs80359726
HLIrs80359726
Exacrs80359726
Varsomers80359726
Maprs80359726
PheGenIrs80359726
hapmaprs80359726
1000 genomesrs80359726
hgdprs80359726
ensemblrs80359726
gopubmedrs80359726
geneviewrs80359726
scholarrs80359726
googlers80359726
pharmgkbrs80359726
gwascentralrs80359726
openSNPrs80359726
23andMers80359726
23andMe allrs80359726
SNP Nexus

SNPshotrs80359726
SNPdbers80359726
MSV3drs80359726
GWAS Ctlgrs80359726
Max Magnitude6
rs80359726, also known as 8941del4, c.8713_8716delTATG and p.Tyr2905_Glu2906?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359726(;)
Alt rs80359726(;)
Reference rs80359726(TATG;TATG)
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.32950887_32950890delTATG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045606.2, RCV000113988.1,