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rs878853298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs878853298(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333384
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853298
dbSNP (old)rs878853298
ClinGenrs878853298
ebirs878853298
HLIrs878853298
Exacrs878853298
Gnomadrs878853298
Varsomers878853298
Maprs878853298
PheGenIrs878853298
Biobankrs878853298
1000 genomesrs878853298
hgdprs878853298
ensemblrs878853298
gopubmedrs878853298
geneviewrs878853298
scholarrs878853298
googlers878853298
pharmgkbrs878853298
gwascentralrs878853298
openSNPrs878853298
23andMers878853298
23andMe allrs878853298
SNP Nexus

SNPshotrs878853298
SNPdbers878853298
MSV3drs878853298
GWAS Ctlgrs878853298
Max Magnitude6
ClinVar
Risk rs878853298(-;-)
Alt rs878853298(-;-)
Reference Rs878853298(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907521delT
CLNSRC
CLNACC RCV000225650.2,