Variant: rs762368691 

    present in Gene: CHRNE;C17orf107
    present in Chromosome: 17
    Position on Chromosome: 4902679
    Alleles of this Variant: -/C

rs762368691 in CHRNE;C17orf107 gene and Myasthenic Syndromes, Congenital PMID 29383513 2018 A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome.

PMID 20562457 2010 Molecular characterisation of congenital myasthenic syndromes in Southern Brazil.

PMID 29054425 2017 Molecular characterization of congenital myasthenic syndromes in Spain.

PMID 9708546 1998 Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor.