RS772302001 MED27

Health Risk Chr 9:131860655
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Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with spasticity
cataracts
and cerebellar hypoplasia
Inborn genetic diseases
Neurodevelopmental disorder with spasticity
cataracts
and cerebellar hypoplasia
Other Variants in MED27
rs1838678412 rs2131076903 rs774276967 rs1024055178
Ask Dr. Hemsworth about this variant