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rs878853585

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853585(A;A)
Make rs878853585(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339062
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853585
ebirs878853585
HLIrs878853585
Exacrs878853585
Varsomers878853585
Maprs878853585
PheGenIrs878853585
hapmaprs878853585
1000 genomesrs878853585
hgdprs878853585
ensemblrs878853585
gopubmedrs878853585
geneviewrs878853585
scholarrs878853585
googlers878853585
pharmgkbrs878853585
gwascentralrs878853585
openSNPrs878853585
23andMers878853585
23andMe allrs878853585
SNP Nexus

SNPshotrs878853585
SNPdbers878853585
MSV3drs878853585
GWAS Ctlgrs878853585
Max Magnitude0
ClinVar
Risk rs878853585(A;A)
Alt rs878853585(A;A)
Reference rs878853585(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.32913199C>A
CLNSRC
CLNACC RCV000227511.1,