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rs878853304

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853304(-;-)
Make rs878853304(-;C)
Make rs878853304(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32362657
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853304
ebirs878853304
HLIrs878853304
Exacrs878853304
Varsomers878853304
Maprs878853304
PheGenIrs878853304
hapmaprs878853304
1000 genomesrs878853304
hgdprs878853304
ensemblrs878853304
gopubmedrs878853304
geneviewrs878853304
scholarrs878853304
googlers878853304
pharmgkbrs878853304
gwascentralrs878853304
openSNPrs878853304
23andMers878853304
23andMe allrs878853304
SNP Nexus

SNPshotrs878853304
SNPdbers878853304
MSV3drs878853304
GWAS Ctlgrs878853304
Max Magnitude0
ClinVar
Risk rs878853304(C;C)
Alt rs878853304(C;C)
Reference rs878853304(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32936794_32936795insC
CLNSRC
CLNACC RCV000225577.1,