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rs80358866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80358866(C;T)
Make rs80358866(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340645
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358866
ebirs80358866
HLIrs80358866
Exacrs80358866
Varsomers80358866
Maprs80358866
PheGenIrs80358866
hapmaprs80358866
1000 genomesrs80358866
hgdprs80358866
ensemblrs80358866
gopubmedrs80358866
geneviewrs80358866
scholarrs80358866
googlers80358866
pharmgkbrs80358866
gwascentralrs80358866
openSNPrs80358866
23andMers80358866
23andMe allrs80358866
SNP Nexus

SNPshotrs80358866
SNPdbers80358866
MSV3drs80358866
GWAS Ctlgrs80358866
Max Magnitude0
ClinVar
Risk rs80358866(T;T)
Alt rs80358866(T;T)
Reference rs80358866(C;C)
Significance Other
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914782C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031613.6, RCV000044889.4, RCV000131379.2,