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rs878853302

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853302(-;-)
Make rs878853302(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32341180
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853302
ebirs878853302
HLIrs878853302
Exacrs878853302
Varsomers878853302
Maprs878853302
PheGenIrs878853302
hapmaprs878853302
1000 genomesrs878853302
hgdprs878853302
ensemblrs878853302
gopubmedrs878853302
geneviewrs878853302
scholarrs878853302
googlers878853302
pharmgkbrs878853302
gwascentralrs878853302
openSNPrs878853302
23andMers878853302
23andMe allrs878853302
SNP Nexus

SNPshotrs878853302
SNPdbers878853302
MSV3drs878853302
GWAS Ctlgrs878853302
Max Magnitude0
ClinVar
Risk rs878853302(;)
Alt rs878853302(;)
Reference rs878853302(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32915317delG
CLNSRC
CLNACC RCV000225578.1,