Variant: rs914395925 

    present in Gene: LOC102723409;LAMA2
    present in Chromosome: 6
    Position on Chromosome: 129502657
    Alleles of this Variant: A/G

rs914395925 in LOC102723409;LAMA2 gene and Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency PMID 24225367 2014 High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency.

PMID 30055037 2018 LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes.