Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853300

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs878853300(-;-)
Make rs878853300(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340943
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853300
ebirs878853300
HLIrs878853300
Exacrs878853300
Varsomers878853300
Maprs878853300
PheGenIrs878853300
hapmaprs878853300
1000 genomesrs878853300
hgdprs878853300
ensemblrs878853300
gopubmedrs878853300
geneviewrs878853300
scholarrs878853300
googlers878853300
pharmgkbrs878853300
gwascentralrs878853300
openSNPrs878853300
23andMers878853300
23andMe allrs878853300
SNP Nexus

SNPshotrs878853300
SNPdbers878853300
MSV3drs878853300
GWAS Ctlgrs878853300
Max Magnitude0
ClinVar
Risk rs878853300(;)
Alt rs878853300(;)
Reference rs878853300(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32915080_32915081delAA
CLNSRC
CLNACC RCV000225666.1,