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rs876658294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar


Make rs876658294(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340951
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658294
dbSNP (old)rs876658294
ClinGenrs876658294
ebirs876658294
HLIrs876658294
Exacrs876658294
Gnomadrs876658294
Varsomers876658294
Maprs876658294
PheGenIrs876658294
Biobankrs876658294
1000 genomesrs876658294
hgdprs876658294
ensemblrs876658294
gopubmedrs876658294
geneviewrs876658294
scholarrs876658294
googlers876658294
pharmgkbrs876658294
gwascentralrs876658294
openSNPrs876658294
23andMers876658294
23andMe allrs876658294
SNP Nexus

SNPshotrs876658294
SNPdbers876658294
MSV3drs876658294
GWAS Ctlgrs876658294
Max Magnitude6
ClinVar
Risk rs876658294(-;-)
Alt rs876658294(-;-)
Reference Rs876658294(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32915088delC
CLNSRC
CLNACC RCV000217392.1, RCV000257079.2,