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rs878853936

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853936(C;G)
Make rs878853936(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925543
GenePTEN
is asnp
is mentioned by
dbSNPrs878853936
ebirs878853936
HLIrs878853936
Exacrs878853936
Varsomers878853936
Maprs878853936
PheGenIrs878853936
hapmaprs878853936
1000 genomesrs878853936
hgdprs878853936
ensemblrs878853936
gopubmedrs878853936
geneviewrs878853936
scholarrs878853936
googlers878853936
pharmgkbrs878853936
gwascentralrs878853936
openSNPrs878853936
23andMers878853936
23andMe allrs878853936
SNP Nexus

SNPshotrs878853936
SNPdbers878853936
MSV3drs878853936
GWAS Ctlgrs878853936
Max Magnitude0
ClinVar
Risk rs878853936(G;G)
Alt rs878853936(G;G)
Reference rs878853936(C;C)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89685300C>G
CLNSRC
CLNACC RCV000226814.1,