RS104894786 DCX

Health Risk Chr X:111410188
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What This Variant Does
"[OMIM:?]
Associated Conditions
Subcortical laminar heterotopia
X-linked
Lissencephaly type 1 due to doublecortin gene mutation
Lissencephaly type 1 due to doublecortin gene mutation
Inborn genetic diseases
Subcortical laminar heterotopia
X-linked
Lissencephaly type 1 due to doublecortin gene mutation
Lissencephaly type 1 due to doublecortin gene mutation
Inborn genetic diseases
Other Variants in DCX
rs104894779 rs104894780 rs104894781 rs122457137 rs104894782 rs1569498597 rs1569497266 rs104894784 rs104894785 rs56030372
Ask Dr. Hemsworth about this variant