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rs587776673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776673(-;-)
Make rs587776673(-;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position87952132
GenePTEN
is asnp
is mentioned by
dbSNPrs587776673
ebirs587776673
HLIrs587776673
Exacrs587776673
Varsomers587776673
Maprs587776673
PheGenIrs587776673
hapmaprs587776673
1000 genomesrs587776673
hgdprs587776673
ensemblrs587776673
gopubmedrs587776673
geneviewrs587776673
scholarrs587776673
googlers587776673
pharmgkbrs587776673
gwascentralrs587776673
openSNPrs587776673
23andMers587776673
23andMe allrs587776673
SNP Nexus

SNPshotrs587776673
SNPdbers587776673
MSV3drs587776673
GWAS Ctlgrs587776673
Max Magnitude0
ClinVar
Risk rs587776673(;)
Alt rs587776673(;)
Reference rs587776673(C;C)
Significance Pathogenic
Disease Proteus-like syndrome PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN Proteus-like syndrome PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89711889delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000008292.3, RCV000008293.3,