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rs878853933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;C) 6.3 PTEN hamartoma tumor syndrome
Make rs878853933(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894077
GenePTEN
is asnp
is mentioned by
dbSNPrs878853933
dbSNP (classic)rs878853933
ClinGenrs878853933
ebirs878853933
HLIrs878853933
Exacrs878853933
Gnomadrs878853933
Varsomers878853933
LitVarrs878853933
Maprs878853933
PheGenIrs878853933
Biobankrs878853933
1000 genomesrs878853933
hgdprs878853933
ensemblrs878853933
geneviewrs878853933
scholarrs878853933
googlers878853933
pharmgkbrs878853933
gwascentralrs878853933
openSNPrs878853933
23andMers878853933
SNPshotrs878853933
SNPdbers878853933
MSV3drs878853933
GWAS Ctlgrs878853933
Max Magnitude6.3
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,