RS587783590 DCX

Health Risk Chr X:111331036
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ectopic tissue
Inborn genetic diseases
Lissencephaly type 1 due to doublecortin gene mutation
Ectopic tissue
Inborn genetic diseases
Lissencephaly type 1 due to doublecortin gene mutation
Other Variants in DCX
rs104894779 rs104894780 rs104894781 rs122457137 rs104894782 rs1569498597 rs1569497266 rs104894784 rs104894785 rs56030372
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