RS1060499733 DHX30
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
7 conditions
Neurodevelopmental disorder with severe motor impairment and absent language
Autism
Intellectual disability
Abnormal cerebral white matter morphology
7 conditions
Neurodevelopmental disorder with severe motor impairment and absent language
Autism
Intellectual disability
Abnormal cerebral white matter morphology
Other Variants in DHX30