Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Loss of catalytically inactive lipid phosphatase myotubularin-related protein 12 impairs myotubularin stability and promotes centronuclear myopathy in zebrafish. 23818870 2013
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Clinical utility gene card for: Centronuclear and myotubular myopathies. 22617344 2012
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT X-linked myotubular myopathy with a novel MTM1 mutation in a Taiwanese child. 19129059 2008
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1. 17005396 2006
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype. 12522554 2003
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT X-linked myotubular myopathy in a family with three adult survivors. 12859411 2003
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Characterization of mutations in fifty North American patients with X-linked myotubular myopathy. 11793470 2002
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC). 12031625 2002
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT MTM1 mutations in X-linked myotubular myopathy. 10790201 2000
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathy. 10502779 1999
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Germline mosaicism in X-linked myotubular myopathy. 10466421 1999
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients. 10063835 1999
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathy. 9829274 1998
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular Center. 9305655 1997
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
0.800 GeneticVariation UNIPROT Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathy. 9285787 1997
dbSNP: rs587783754
rs587783754
Entrez Id: 4534
Gene Symbol: MTM1
MTM1
CUI: C0410203
Disease:
X-linked centronuclear myopathy
G 0.800 CausalMutation CLINVAR