RS774276967 MED27

Health Risk Chr 9:131860603
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Associated Conditions
Neurodevelopmental disorder with spasticity
cataracts
and cerebellar hypoplasia
Severe myoclonic epilepsy in infancy
Neurodevelopmental disorder with spasticity
cataracts
and cerebellar hypoplasia
Severe myoclonic epilepsy in infancy
Other Variants in MED27
rs1838678412 rs2131076903 rs1024055178 rs772302001
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