Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5913
Gene Symbol: RAPSN
RAPSN 		0.600 CausalMutation disease CLINVAR Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes. 12807980 2003
Entrez Id: 5913
Gene Symbol: RAPSN
RAPSN 		0.600 GeneticVariation disease UNIPROT Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome. 11791205 2002
Entrez Id: 5913
Gene Symbol: RAPSN
RAPSN 		0.600 CausalMutation disease CLINVAR Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome. 11791205 2002