RS869312676 OPHN1

Health Risk Chr X:68063977
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
X-linked intellectual disability-cerebellar hypoplasia syndrome
X-linked intellectual disability-cerebellar hypoplasia syndrome
Other Variants in OPHN1
rs1569211016 rs1569243931 rs137854493 rs1569244467 rs143713841 rs375325266 rs587784234 rs727504062 rs150084635 rs368803937
Ask Dr. Hemsworth about this variant