RS1561314246 MAP1B
Upload your DNA to see your genotype for this variant.
Associated Conditions
White matter deficit
Periventricular nodular heterotopia
Cognitive impairment
Hypoplasia of the corpus callosum
Periventricular nodular heterotopia 9
White matter deficit
Periventricular nodular heterotopia
Cognitive impairment
Hypoplasia of the corpus callosum
Periventricular nodular heterotopia 9
Other Variants in MAP1B