RS398124204 FOXG1

Health Risk Chr 14:28767733
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What This Variant Does
"CLNSIG=5
Associated Conditions
FOXG1 disorder
Inborn genetic diseases
Abnormal cerebral morphology
FOXG1-related disorder
FOXG1 disorder
FOXG1 disorder
FOXG1 disorder
Inborn genetic diseases
Abnormal cerebral morphology
FOXG1-related disorder
FOXG1 disorder
FOXG1 disorder
Other Variants in FOXG1
rs121913678 rs267606826 rs267606828 rs267606827 rs138747073 rs587783629 rs587783631 rs587783635 rs587783636 rs587783638
Ask Dr. Hemsworth about this variant