RS267606826 FOXG1

Health Risk Chr 14:28767903
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
FOXG1 disorder
Inborn genetic diseases
FOXG1 disorder
Strabismus
Abnormal optic nerve morphology
Global developmental delay
Axial hypotonia
Stereotypic movement disorder
FOXG1 disorder
Inborn genetic diseases
FOXG1 disorder
Strabismus
Abnormal optic nerve morphology
Global developmental delay
Axial hypotonia
Other Variants in FOXG1
rs121913678 rs267606828 rs267606827 rs138747073 rs398124204 rs587783629 rs587783631 rs587783635 rs587783636 rs587783638
Ask Dr. Hemsworth about this variant