RS1921403332 DCX

Health Risk Chr X:111333050
Upload your DNA to see your genotype for this variant.
Associated Conditions
Lissencephaly type 1 due to doublecortin gene mutation
Subcortical laminar heterotopia
X-linked
Lissencephaly type 1 due to doublecortin gene mutation
Subcortical laminar heterotopia
X-linked
Other Variants in DCX
rs104894779 rs104894780 rs104894781 rs122457137 rs104894782 rs1569498597 rs1569497266 rs104894784 rs104894785 rs56030372
Ask Dr. Hemsworth about this variant