RS796052231 DDX3X

Health Risk Chr X:41345280
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
X-linked 102
Congenital cerebellar hypoplasia
Inborn genetic diseases
Medulloblastoma WNT activated
Intellectual disability
X-linked 102
Congenital cerebellar hypoplasia
Inborn genetic diseases
Medulloblastoma WNT activated
Other Variants in DDX3X
rs1555951992 rs796052224 rs796052232 rs796052238 rs796052227 rs796052234 rs796052235 rs796052236 rs796052230 rs796052226
Ask Dr. Hemsworth about this variant