RS1563183469 AUTS2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Multiple congenital anomalies
Corpus callosum
agenesis of
Autism spectrum disorder due to AUTS2 deficiency
Congenital cerebellar hypoplasia
Multiple congenital anomalies
Corpus callosum
agenesis of
Autism spectrum disorder due to AUTS2 deficiency
Congenital cerebellar hypoplasia
Other Variants in AUTS2