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rs878853944

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853944(G;T)
Make rs878853944(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87960969
GenePTEN
is asnp
is mentioned by
dbSNPrs878853944
ebirs878853944
HLIrs878853944
Exacrs878853944
Varsomers878853944
Maprs878853944
PheGenIrs878853944
hapmaprs878853944
1000 genomesrs878853944
hgdprs878853944
ensemblrs878853944
gopubmedrs878853944
geneviewrs878853944
scholarrs878853944
googlers878853944
pharmgkbrs878853944
gwascentralrs878853944
openSNPrs878853944
23andMers878853944
23andMe allrs878853944
SNP Nexus

SNPshotrs878853944
SNPdbers878853944
MSV3drs878853944
GWAS Ctlgrs878853944
Max Magnitude0
ClinVar
Risk rs878853944(T;T)
Alt rs878853944(T;T)
Reference rs878853944(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89720726G>T
CLNSRC
CLNACC RCV000234288.1,