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rs80359776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359776(-;-)
Make rs80359776(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398381
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359776
ebirs80359776
HLIrs80359776
Exacrs80359776
Varsomers80359776
Maprs80359776
PheGenIrs80359776
hapmaprs80359776
1000 genomesrs80359776
hgdprs80359776
ensemblrs80359776
gopubmedrs80359776
geneviewrs80359776
scholarrs80359776
googlers80359776
pharmgkbrs80359776
gwascentralrs80359776
openSNPrs80359776
23andMers80359776
23andMe allrs80359776
SNP Nexus

SNPshotrs80359776
SNPdbers80359776
MSV3drs80359776
GWAS Ctlgrs80359776
Max Magnitude0
ClinVar
Risk rs80359776(;)
Alt rs80359776(;)
Reference rs80359776(G;G)
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.32972518delG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045907.2, RCV000112818.1,