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rs80359021

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359021(C;C)
Make rs80359021(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32362657
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359021
ebirs80359021
HLIrs80359021
Exacrs80359021
Varsomers80359021
Maprs80359021
PheGenIrs80359021
hapmaprs80359021
1000 genomesrs80359021
hgdprs80359021
ensemblrs80359021
gopubmedrs80359021
geneviewrs80359021
scholarrs80359021
googlers80359021
pharmgkbrs80359021
gwascentralrs80359021
openSNPrs80359021
23andMers80359021
23andMe allrs80359021
SNP Nexus

SNPshotrs80359021
SNPdbers80359021
MSV3drs80359021
GWAS Ctlgrs80359021
Max Magnitude0
ClinVar
Risk rs80359021(C;C)
Alt rs80359021(C;C)
Reference rs80359021(T;T)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32936794T>C
CLNSRC
CLNACC RCV000045351.2, RCV000083142.3, RCV000162550.1,