Variant: rs1057516046 

    present in Gene: ACTG2
    present in Chromosome: 2
    Position on Chromosome: 73913646
    Alleles of this Variant: G/A

rs1057516046 in ACTG2 gene and Decreased peristalsis PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1057516046 in ACTG2 gene and Dilatation of the bladder PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1057516046 in ACTG2 gene and Visceral Myopathy PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.