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rs876658153

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658153(G;T)
Make rs876658153(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925558
GenePTEN
is asnp
is mentioned by
dbSNPrs876658153
ebirs876658153
HLIrs876658153
Exacrs876658153
Varsomers876658153
Maprs876658153
PheGenIrs876658153
hapmaprs876658153
1000 genomesrs876658153
hgdprs876658153
ensemblrs876658153
gopubmedrs876658153
geneviewrs876658153
scholarrs876658153
googlers876658153
pharmgkbrs876658153
gwascentralrs876658153
openSNPrs876658153
23andMers876658153
23andMe allrs876658153
SNP Nexus

SNPshotrs876658153
SNPdbers876658153
MSV3drs876658153
GWAS Ctlgrs876658153
Max Magnitude0
ClinVar
Risk rs876658153(T;T)
Alt rs876658153(T;T)
Reference rs876658153(G;G)
Significance Probable-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.89685315G>T
CLNSRC
CLNACC RCV000213295.1,