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rs876658589

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658589(-;-)
Make rs876658589(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332612
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658589
ebirs876658589
HLIrs876658589
Exacrs876658589
Varsomers876658589
Maprs876658589
PheGenIrs876658589
hapmaprs876658589
1000 genomesrs876658589
hgdprs876658589
ensemblrs876658589
gopubmedrs876658589
geneviewrs876658589
scholarrs876658589
googlers876658589
pharmgkbrs876658589
gwascentralrs876658589
openSNPrs876658589
23andMers876658589
23andMe allrs876658589
SNP Nexus

SNPshotrs876658589
SNPdbers876658589
MSV3drs876658589
GWAS Ctlgrs876658589
Max Magnitude0
ClinVar
Risk rs876658589(;)
Alt rs876658589(;)
Reference rs876658589(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32906749delT
CLNSRC
CLNACC RCV000218138.1,