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rs878853569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;GA) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs878853569(GA;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337837
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853569
dbSNP (old)rs878853569
ClinGenrs878853569
ebirs878853569
HLIrs878853569
Exacrs878853569
Varsomers878853569
Maprs878853569
PheGenIrs878853569
Biobankrs878853569
1000 genomesrs878853569
hgdprs878853569
ensemblrs878853569
gopubmedrs878853569
geneviewrs878853569
scholarrs878853569
googlers878853569
pharmgkbrs878853569
gwascentralrs878853569
openSNPrs878853569
23andMers878853569
23andMe allrs878853569
SNP Nexus

SNPshotrs878853569
SNPdbers878853569
MSV3drs878853569
GWAS Ctlgrs878853569
Max Magnitude6
ClinVar
Risk rs878853569(AG;AG)
Alt rs878853569(AG;AG)
Reference Rs878853569(-;-)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911973_32911974dupGA
CLNSRC
CLNACC RCV000234119.2, RCV000256803.2,