LAMA2, laminin subunit alpha 2, 3908

N. diseases: 167; N. variants: 127
Disease: Congenital muscular dystrophy (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562530132
rs1562530132
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C0699743
Disease:
Congenital muscular dystrophy (disorder) 		C 0.700 GeneticVariation CLINVAR