Variant: rs587777332 

    present in Gene: MIR6890;QARS1
    present in Chromosome: 3
    Position on Chromosome: 49100049
    Alleles of this Variant: G/A

rs587777332 in MIR6890;QARS1 gene and MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY PMID 26869582 2016 The crystal structure of human GlnRS provides basis for the development of neurological disorders.

PMID 24656866 2014 Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.