Variant: rs1209130981 

    present in Gene: LAMA2
    present in Chromosome: 6
    Position on Chromosome: 129149008
    Alleles of this Variant: AT/-

rs1209130981 in LAMA2 gene and Muscle hypotonia PMID 24223650 2013 Merosin-deficient congenital muscular dystrophy type 1A: A case report.

PMID 21953594 2011 Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations.

PMID 12552556 2003 Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.

PMID 26304763 2016 Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy.

PMID 20207543 2010 Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations.

PMID 18700894 2008 LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.