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rs878853561

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853561(G;T)
Make rs878853561(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336594
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853561
ebirs878853561
HLIrs878853561
Exacrs878853561
Varsomers878853561
Maprs878853561
PheGenIrs878853561
hapmaprs878853561
1000 genomesrs878853561
hgdprs878853561
ensemblrs878853561
gopubmedrs878853561
geneviewrs878853561
scholarrs878853561
googlers878853561
pharmgkbrs878853561
gwascentralrs878853561
openSNPrs878853561
23andMers878853561
23andMe allrs878853561
SNP Nexus

SNPshotrs878853561
SNPdbers878853561
MSV3drs878853561
GWAS Ctlgrs878853561
Max Magnitude0
ClinVar
Risk rs878853561(T;T)
Alt rs878853561(T;T)
Reference rs878853561(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32910731G>T
CLNSRC
CLNACC RCV000229810.1,