RS1555321402 FOXG1

Health Risk Chr 14:28768345
Upload your DNA to see your genotype for this variant.
Associated Conditions
Primary microcephaly
Severe intellectual disability
Aplasia/Hypoplasia of the corpus callosum
Primary microcephaly
Severe intellectual disability
Aplasia/Hypoplasia of the corpus callosum
Other Variants in FOXG1
rs121913678 rs267606826 rs267606828 rs267606827 rs138747073 rs398124204 rs587783629 rs587783631 rs587783635 rs587783636
Ask Dr. Hemsworth about this variant