TRIM2, tripartite motif containing 2, 23321

N. diseases: 44; N. variants: 6
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777063
rs587777063
Entrez Id: 23321
Gene Symbol: TRIM2
TRIM2
CUI: C3809655
Disease:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R 		0.800 GeneticVariation UNIPROT Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy. 23562820 2013
dbSNP: rs587777063
rs587777063
Entrez Id: 23321
Gene Symbol: TRIM2
TRIM2
CUI: C3809655
Disease:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R 		T 0.800 CausalMutation CLINVAR