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rs80359066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359066(C;C)
Make rs80359066(C;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position32363390
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359066
ebirs80359066
HLIrs80359066
Exacrs80359066
Varsomers80359066
Maprs80359066
PheGenIrs80359066
hapmaprs80359066
1000 genomesrs80359066
hgdprs80359066
ensemblrs80359066
gopubmedrs80359066
geneviewrs80359066
scholarrs80359066
googlers80359066
pharmgkbrs80359066
gwascentralrs80359066
openSNPrs80359066
23andMers80359066
23andMe allrs80359066
SNP Nexus

SNPshotrs80359066
SNPdbers80359066
MSV3drs80359066
GWAS Ctlgrs80359066
Max Magnitude0
ClinVar
Risk rs80359066(C;C)
Alt rs80359066(C;C)
Reference rs80359066(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32937527G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000113886.1, RCV000131217.2, RCV000160150.2,