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rs878853287

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853287(A;G)
Make rs878853287(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32330917
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853287
ebirs878853287
HLIrs878853287
Exacrs878853287
Varsomers878853287
Maprs878853287
PheGenIrs878853287
hapmaprs878853287
1000 genomesrs878853287
hgdprs878853287
ensemblrs878853287
gopubmedrs878853287
geneviewrs878853287
scholarrs878853287
googlers878853287
pharmgkbrs878853287
gwascentralrs878853287
openSNPrs878853287
23andMers878853287
23andMe allrs878853287
SNP Nexus

SNPshotrs878853287
SNPdbers878853287
MSV3drs878853287
GWAS Ctlgrs878853287
Max Magnitude0
ClinVar
Risk rs878853287(G;G)
Alt rs878853287(G;G)
Reference rs878853287(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32905054A>G
CLNSRC
CLNACC RCV000225520.1,