Variant: rs587777677 

    present in Gene: LAMA1
    present in Chromosome: 18
    Position on Chromosome: 7050692
    Alleles of this Variant: A/C

rs587777677 in LAMA1 gene and Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome PMID 25105227 2014 Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy.