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rs878853933

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853933(-;-)
Make rs878853933(-;C)
Make rs878853933(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894077
GenePTEN
is asnp
is mentioned by
dbSNPrs878853933
ebirs878853933
HLIrs878853933
Exacrs878853933
Varsomers878853933
Maprs878853933
PheGenIrs878853933
hapmaprs878853933
1000 genomesrs878853933
hgdprs878853933
ensemblrs878853933
gopubmedrs878853933
geneviewrs878853933
scholarrs878853933
googlers878853933
pharmgkbrs878853933
gwascentralrs878853933
openSNPrs878853933
23andMers878853933
23andMe allrs878853933
SNP Nexus

SNPshotrs878853933
SNPdbers878853933
MSV3drs878853933
GWAS Ctlgrs878853933
Max Magnitude0
ClinVar
Risk rs878853933(C;C)
Alt rs878853933(C;C)
Reference rs878853933(;)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89653834dupC
CLNSRC
CLNACC RCV000226096.1,