RS145451123 AFG2B

Health Risk Chr 15:45402956
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Associated Conditions
SPATA5L1-associated disorder
Hearing loss
autosomal recessive 119
See cases
Neurodevelopmental disorder with hearing loss and spasticity
Neurodevelopmental delay
AFG2B-related disorder
Inborn genetic diseases
SPATA5L1-related disorder
SPATA5L1-associated disorder
Hearing loss
autosomal recessive 119
See cases
Neurodevelopmental disorder with hearing loss and spasticity
Neurodevelopmental delay
Other Variants in AFG2B
rs777812455 rs148815842 rs747177622 rs747249958 rs765912979 rs763343580 rs778481503 rs1212383243 rs1230836596 rs34675173
Ask Dr. Hemsworth about this variant