Variant: rs749797580 

    present in Gene: LAMA2;LOC102723409
    present in Chromosome: 6
    Position on Chromosome: 129516273
    Alleles of this Variant: A/T

rs749797580 in LAMA2;LOC102723409 gene and Muscular dystrophy congenital, merosin negative PMID 10619025 1999 The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin.

PMID 10747011 2000 Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin.

PMID 10022829 1999 Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins.