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rs878853941

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853941(-;-)
Make rs878853941(-;T)
Make rs878853941(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87952170
GenePTEN
is asnp
is mentioned by
dbSNPrs878853941
ebirs878853941
HLIrs878853941
Exacrs878853941
Varsomers878853941
Maprs878853941
PheGenIrs878853941
hapmaprs878853941
1000 genomesrs878853941
hgdprs878853941
ensemblrs878853941
gopubmedrs878853941
geneviewrs878853941
scholarrs878853941
googlers878853941
pharmgkbrs878853941
gwascentralrs878853941
openSNPrs878853941
23andMers878853941
23andMe allrs878853941
SNP Nexus

SNPshotrs878853941
SNPdbers878853941
MSV3drs878853941
GWAS Ctlgrs878853941
Max Magnitude0
ClinVar
Risk rs878853941(T;T)
Alt rs878853941(T;T)
Reference rs878853941(;)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89711927dupT
CLNSRC
CLNACC RCV000230682.1,