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rs80359772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359772(-;-)
Make rs80359772(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398179
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359772
ebirs80359772
HLIrs80359772
Exacrs80359772
Varsomers80359772
Maprs80359772
PheGenIrs80359772
hapmaprs80359772
1000 genomesrs80359772
hgdprs80359772
ensemblrs80359772
gopubmedrs80359772
geneviewrs80359772
scholarrs80359772
googlers80359772
pharmgkbrs80359772
gwascentralrs80359772
openSNPrs80359772
23andMers80359772
23andMe allrs80359772
SNP Nexus

SNPshotrs80359772
SNPdbers80359772
MSV3drs80359772
GWAS Ctlgrs80359772
Max Magnitude0
ClinVar
Risk rs80359772(;)
Alt rs80359772(;)
Reference rs80359772(T;T)
Significance 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.32972316delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045883.2, RCV000114150.1, RCV000130019.2,