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rs876658837

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658837(-;-)
Make rs876658837(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87961041
GenePTEN
is asnp
is mentioned by
dbSNPrs876658837
ebirs876658837
HLIrs876658837
Exacrs876658837
Varsomers876658837
Maprs876658837
PheGenIrs876658837
hapmaprs876658837
1000 genomesrs876658837
hgdprs876658837
ensemblrs876658837
gopubmedrs876658837
geneviewrs876658837
scholarrs876658837
googlers876658837
pharmgkbrs876658837
gwascentralrs876658837
openSNPrs876658837
23andMers876658837
23andMe allrs876658837
SNP Nexus

SNPshotrs876658837
SNPdbers876658837
MSV3drs876658837
GWAS Ctlgrs876658837
Max Magnitude0
ClinVar
Risk rs876658837(;)
Alt rs876658837(;)
Reference rs876658837(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89720798delG
CLNSRC
CLNACC RCV000217505.1,