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rs878853559

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853559(C;T)
Make rs878853559(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336450
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853559
ebirs878853559
HLIrs878853559
Exacrs878853559
Varsomers878853559
Maprs878853559
PheGenIrs878853559
hapmaprs878853559
1000 genomesrs878853559
hgdprs878853559
ensemblrs878853559
gopubmedrs878853559
geneviewrs878853559
scholarrs878853559
googlers878853559
pharmgkbrs878853559
gwascentralrs878853559
openSNPrs878853559
23andMers878853559
23andMe allrs878853559
SNP Nexus

SNPshotrs878853559
SNPdbers878853559
MSV3drs878853559
GWAS Ctlgrs878853559
Max Magnitude0
ClinVar
Risk rs878853559(T;T)
Alt rs878853559(T;T)
Reference rs878853559(C;C)
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.32910587C>T
CLNSRC
CLNACC RCV000229702.1,