RS766745103 TBC1D24

Health Risk Chr 16:2497099
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Associated Conditions
Familial infantile myoclonic epilepsy
Inborn genetic diseases
Developmental and epileptic encephalopathy
1
Autosomal dominant nonsyndromic hearing loss 65
Familial infantile myoclonic epilepsy
Inborn genetic diseases
Developmental and epileptic encephalopathy
1
Autosomal dominant nonsyndromic hearing loss 65
Other Variants in TBC1D24
rs267607103 rs267607105 rs267607104 rs398122941 rs397514713 rs397514714 rs398122965 rs398122966 rs201257588 rs398122967
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