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rs878853619

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853619(-;-)
Make rs878853619(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394702
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853619
ebirs878853619
HLIrs878853619
Exacrs878853619
Varsomers878853619
Maprs878853619
PheGenIrs878853619
hapmaprs878853619
1000 genomesrs878853619
hgdprs878853619
ensemblrs878853619
gopubmedrs878853619
geneviewrs878853619
scholarrs878853619
googlers878853619
pharmgkbrs878853619
gwascentralrs878853619
openSNPrs878853619
23andMers878853619
23andMe allrs878853619
SNP Nexus

SNPshotrs878853619
SNPdbers878853619
MSV3drs878853619
GWAS Ctlgrs878853619
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs878853619(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.32968839delC
CLNSRC
CLNACC RCV000232594.1,