RS587783592 DCX

Health Risk Chr X:111330943
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Ectopic tissue
Lissencephaly
Lissencephaly type 1 due to doublecortin gene mutation
Inborn genetic diseases
Ectopic tissue
Lissencephaly
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