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rs876658551

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658551(G;T)
Make rs876658551(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32344557
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658551
ebirs876658551
HLIrs876658551
Exacrs876658551
Varsomers876658551
Maprs876658551
PheGenIrs876658551
hapmaprs876658551
1000 genomesrs876658551
hgdprs876658551
ensemblrs876658551
gopubmedrs876658551
geneviewrs876658551
scholarrs876658551
googlers876658551
pharmgkbrs876658551
gwascentralrs876658551
openSNPrs876658551
23andMers876658551
23andMe allrs876658551
SNP Nexus

SNPshotrs876658551
SNPdbers876658551
MSV3drs876658551
GWAS Ctlgrs876658551
Max Magnitude0
ClinVar
Risk rs876658551(T;T)
Alt rs876658551(T;T)
Reference rs876658551(G;G)
Significance Probable-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.32918694G>T
CLNSRC
CLNACC RCV000214372.1,