LMLN, leishmanolysin like peptidase, 89782

N. diseases: 138; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9813476
rs9813476 		3 197992314 intron variant C/T snv 3.7E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2017 2017
dbSNP: rs9813476
rs9813476 		3 197992314 intron variant C/T snv 3.7E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1239669755
rs1239669755 		0.851 0.080 3 197960384 missense variant C/T snv
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.030 1.000 3 2008 2010
dbSNP: rs1239669755
rs1239669755 		0.851 0.080 3 197960384 missense variant C/T snv
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2013 2013
dbSNP: rs1239669755
rs1239669755 		0.851 0.080 3 197960384 missense variant C/T snv
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1239669755
rs1239669755 		0.851 0.080 3 197960384 missense variant C/T snv
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2010 2010