DNM2, dynamin 2, 1785

N. diseases: 178; N. variants: 30
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199927590
rs199927590
Entrez Id: 1785
Gene Symbol: DNM2
DNM2
CUI: C0007959
Disease:
Charcot-Marie-Tooth Disease
G 0.700 GeneticVariation CLINVAR Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing. 25025039 2014
dbSNP: rs121909088
rs121909088
Entrez Id: 1785
Gene Symbol: DNM2
DNM2
CUI: C0007959
Disease:
Charcot-Marie-Tooth Disease
0.010 GeneticVariation BEFREE We studied the clinical, haematological, electrophysiological and sural nerve biopsy findings in 34 patients belonging to six unrelated dominant intermediate Charcot-Marie-Tooth neuropathy type B families in whom a dynamin 2 mutation had been identified: Gly358Arg (Spain); Asp551_Glu553del; Lys550fs (North America); Lys558del (Belgium); Lys558Glu (Australia, the Netherlands) and Thr855_Ile856del (Belgium). 19502294 2009
dbSNP: rs267606772
rs267606772
Entrez Id: 1785
Gene Symbol: DNM2
DNM2
CUI: C0007959
Disease:
Charcot-Marie-Tooth Disease
0.010 GeneticVariation BEFREE We studied the clinical, haematological, electrophysiological and sural nerve biopsy findings in 34 patients belonging to six unrelated dominant intermediate Charcot-Marie-Tooth neuropathy type B families in whom a dynamin 2 mutation had been identified: Gly358Arg (Spain); Asp551_Glu553del; Lys550fs (North America); Lys558del (Belgium); Lys558Glu (Australia, the Netherlands) and Thr855_Ile856del (Belgium). 19502294 2009