Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells. 27477328 2017
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR Characteristic brain magnetic resonance imaging pattern in patients with macrocephaly and PTEN mutations. 24375884 2014
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR Elevated plasma succinate in PTEN, SDHB, and SDHD mutation-positive individuals. 22261759 2012
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes. 21828076 2011
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR In vivo functional analysis of the counterbalance of hyperactive phosphatidylinositol 3-kinase p110 catalytic oncoproteins by the tumor suppressor PTEN. 17942903 2007
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults. 14566704 2003
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 GeneticVariation CLINVAR PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. 10400993 1999
dbSNP: rs587782350
rs587782350
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1866398
Disease:
Proteus-Like Syndrome (disorder)
T 0.700 CausalMutation CLINVAR