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rs878853605

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853605(-;-)
Make rs878853605(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32357797
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853605
ebirs878853605
HLIrs878853605
Exacrs878853605
Varsomers878853605
Maprs878853605
PheGenIrs878853605
hapmaprs878853605
1000 genomesrs878853605
hgdprs878853605
ensemblrs878853605
gopubmedrs878853605
geneviewrs878853605
scholarrs878853605
googlers878853605
pharmgkbrs878853605
gwascentralrs878853605
openSNPrs878853605
23andMers878853605
23andMe allrs878853605
SNP Nexus

SNPshotrs878853605
SNPdbers878853605
MSV3drs878853605
GWAS Ctlgrs878853605
Max Magnitude0
ClinVar
Risk rs878853605(;)
Alt rs878853605(;)
Reference rs878853605(A;A)
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.32931934delA
CLNSRC
CLNACC RCV000229882.1,