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rs878853937

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853937(A;A)
Make rs878853937(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925559
GenePTEN
is asnp
is mentioned by
dbSNPrs878853937
ebirs878853937
HLIrs878853937
Exacrs878853937
Varsomers878853937
Maprs878853937
PheGenIrs878853937
hapmaprs878853937
1000 genomesrs878853937
hgdprs878853937
ensemblrs878853937
gopubmedrs878853937
geneviewrs878853937
scholarrs878853937
googlers878853937
pharmgkbrs878853937
gwascentralrs878853937
openSNPrs878853937
23andMers878853937
23andMe allrs878853937
SNP Nexus

SNPshotrs878853937
SNPdbers878853937
MSV3drs878853937
GWAS Ctlgrs878853937
Max Magnitude0
ClinVar
Risk rs878853937(A;A)
Alt rs878853937(A;A)
Reference rs878853937(T;T)
Significance Probable-Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89685316T>A
CLNSRC
CLNACC RCV000229236.1,