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rs878853942

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853942(-;-)
Make rs878853942(-;AT)
Make rs878853942(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87957976
GenePTEN
is asnp
is mentioned by
dbSNPrs878853942
ebirs878853942
HLIrs878853942
Exacrs878853942
Varsomers878853942
Maprs878853942
PheGenIrs878853942
hapmaprs878853942
1000 genomesrs878853942
hgdprs878853942
ensemblrs878853942
gopubmedrs878853942
geneviewrs878853942
scholarrs878853942
googlers878853942
pharmgkbrs878853942
gwascentralrs878853942
openSNPrs878853942
23andMers878853942
23andMe allrs878853942
SNP Nexus

SNPshotrs878853942
SNPdbers878853942
MSV3drs878853942
GWAS Ctlgrs878853942
Max Magnitude0
ClinVar
Risk rs878853942(AT;AT)
Alt rs878853942(AT;AT)
Reference rs878853942(;)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89717732_89717733dupAT
CLNSRC
CLNACC RCV000234527.1,