Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 GeneticVariation disease CLINVAR Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. 30301903 2018
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 GeneticVariation disease CLINVAR LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes. 30055037 2018
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 GeneticVariation disease CLINVAR High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency. 24225367 2014
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 GeneticVariation disease CLINVAR Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. 20207543 2010
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 CausalMutation disease CLINVAR