Variant: rs1156410888 

    present in Gene: TNNT1
    present in Chromosome: 19
    Position on Chromosome: 55137214
    Alleles of this Variant: T/C

rs1156410888 in TNNT1 gene and NEMALINE MYOPATHY 5 PMID 10952871 2000 A novel nemaline myopathy in the Amish caused by a mutation in troponin T1.

PMID 24689076 2014 Nemaline myopathy caused byTNNT1 mutations in a Dutch pedigree.

PMID 25430424 2015 Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish.