RS1599017933 CDH2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Axon pathfinding
cardiac
ocular and genital defects
Corpus callosum
agenesis of
Syndromic neurodevelopmental disorder
Axon pathfinding
cardiac
ocular and genital defects
Corpus callosum
agenesis of
Syndromic neurodevelopmental disorder
Other Variants in CDH2