Variant: rs1415944134 

    present in Gene: LAMA2
    present in Chromosome: 6
    Position on Chromosome: 129393095
    Alleles of this Variant: G/-;GG

rs1415944134 in LAMA2 gene and Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency PMID 30301903 2018 Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy.

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