Variant: rs886042805 

    present in Gene: TTC7A
    present in Chromosome: 2
    Position on Chromosome: 46950464
    Alleles of this Variant: G/T

rs886042805 in TTC7A gene and Congenital atresia of colon PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs886042805 in TTC7A gene and Congenital atresia of ileum PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs886042805 in TTC7A gene and Congenital pyloric atresia PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs886042805 in TTC7A gene and Jejunal Atresia PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs886042805 in TTC7A gene and Multiple gastrointestinal atresias (disorder) PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.