RS797045586 FOXP1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Inborn genetic diseases
Intellectual disability
See cases
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Inborn genetic diseases
Intellectual disability
See cases
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Other Variants in FOXP1