RS56030372 DCX

Health Risk Chr X:111401108
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What This Variant Does
"[OMIM:?]
Associated Conditions
Subcortical laminar heterotopia
X-linked
Lissencephaly type 1 due to doublecortin gene mutation
Ectopic tissue
Abnormal cerebral morphology
Inborn genetic diseases
Subcortical laminar heterotopia
X-linked
Lissencephaly type 1 due to doublecortin gene mutation
Ectopic tissue
Abnormal cerebral morphology
Inborn genetic diseases
Other Variants in DCX
rs104894779 rs104894780 rs104894781 rs122457137 rs104894782 rs1569498597 rs1569497266 rs104894784 rs104894785 rs104894786
Ask Dr. Hemsworth about this variant