MAG, myelin associated glycoprotein, 4099

N. diseases: 106; N. variants: 9
Disease: SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2301600
rs2301600
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site. 27606346 2016
dbSNP: rs587777229
rs587777229
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site. 27606346 2016
dbSNP: rs2301600
rs2301600
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder. 26179919 2015
dbSNP: rs587777229
rs587777229
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder. 26179919 2015
dbSNP: rs2301600
rs2301600
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. 24482476 2014
dbSNP: rs587777229
rs587777229
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. 24482476 2014
dbSNP: rs2301600
rs2301600
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		G 0.800 CausalMutation CLINVAR
dbSNP: rs587777229
rs587777229
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		G 0.800 CausalMutation CLINVAR
dbSNP: rs762045079
rs762045079
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation UNIPROT Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site. 27606346 2016
dbSNP: rs762045079
rs762045079
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation UNIPROT Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder. 26179919 2015
dbSNP: rs762045079
rs762045079
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation UNIPROT Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. 24482476 2014
dbSNP: rs771777424
rs771777424
Entrez Id: 4099
Gene Symbol: MAG
MAG
CUI: C4225250
Disease:
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		CCTGAG 0.700 CausalMutation CLINVAR