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rs878853608

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853608(-;-)
Make rs878853608(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32363425
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853608
ebirs878853608
HLIrs878853608
Exacrs878853608
Varsomers878853608
Maprs878853608
PheGenIrs878853608
hapmaprs878853608
1000 genomesrs878853608
hgdprs878853608
ensemblrs878853608
gopubmedrs878853608
geneviewrs878853608
scholarrs878853608
googlers878853608
pharmgkbrs878853608
gwascentralrs878853608
openSNPrs878853608
23andMers878853608
23andMe allrs878853608
SNP Nexus

SNPshotrs878853608
SNPdbers878853608
MSV3drs878853608
GWAS Ctlgrs878853608
Max Magnitude0
ClinVar
Risk rs878853608(;)
Alt rs878853608(;)
Reference rs878853608(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.32937562delG
CLNSRC
CLNACC RCV000228116.1,