LMLN, leishmanolysin like peptidase, 89782

N. diseases: 138; N. variants: 2
Disease: Amyotrophic Lateral Sclerosis, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1239669755
rs1239669755
Entrez Id: 84223;89782
Gene Symbol: IQCG;LMLN
IQCG;LMLN
CUI: C4551993
Disease:
Amyotrophic Lateral Sclerosis, Familial 		0.010 GeneticVariation BEFREE The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis. 20377183 2010