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rs876658589

From SNPedia

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


Make rs876658589(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332612
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658589
dbSNP (old)rs876658589
ClinGenrs876658589
ebirs876658589
HLIrs876658589
Exacrs876658589
Varsomers876658589
Maprs876658589
PheGenIrs876658589
Biobankrs876658589
1000 genomesrs876658589
hgdprs876658589
ensemblrs876658589
gopubmedrs876658589
geneviewrs876658589
scholarrs876658589
googlers876658589
pharmgkbrs876658589
gwascentralrs876658589
openSNPrs876658589
23andMers876658589
23andMe allrs876658589
SNP Nexus

SNPshotrs876658589
SNPdbers876658589
MSV3drs876658589
GWAS Ctlgrs876658589
Max Magnitude6
ClinVar
Risk rs876658589(-;-)
Alt rs876658589(-;-)
Reference Rs876658589(T;T)
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.32906749delT
CLNSRC
CLNACC RCV000218138.1, RCV000256982.2,