Condition: Decreased peristalsis
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.
rs1557043622
in
SLC35A2
gene and
Decreased peristalsis
PMID 30817854
2019 SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.