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rs878853595

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853595(-;-)
Make rs878853595(-;G)
Make rs878853595(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340588
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853595
ebirs878853595
HLIrs878853595
Exacrs878853595
Varsomers878853595
Maprs878853595
PheGenIrs878853595
hapmaprs878853595
1000 genomesrs878853595
hgdprs878853595
ensemblrs878853595
gopubmedrs878853595
geneviewrs878853595
scholarrs878853595
googlers878853595
pharmgkbrs878853595
gwascentralrs878853595
openSNPrs878853595
23andMers878853595
23andMe allrs878853595
SNP Nexus

SNPshotrs878853595
SNPdbers878853595
MSV3drs878853595
GWAS Ctlgrs878853595
Max Magnitude0
ClinVar
Risk rs878853595(G;G)
Alt rs878853595(G;G)
Reference rs878853595(;)
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.32914725dupG
CLNSRC
CLNACC RCV000230064.1,