LAMA2, laminin subunit alpha 2, 3908

N. diseases: 167; N. variants: 127
Disease: Muscular dystrophy congenital, merosin negative ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs374403765
rs374403765
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.700 GeneticVariation CLINVAR Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. 9674786 1998