RS1064793130 FOXP1

Health Risk Chr 3:70977935
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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-severe speech delay-mild dysmorphism syndrome
Inborn genetic diseases
Other Variants in FOXP1
rs112795301 rs398124429 rs786200948 rs587777855 rs372403441 rs794727155 rs797044652 rs794727215 rs794727216 rs749771909
Ask Dr. Hemsworth about this variant