RS267607105 TBC1D24
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial infantile myoclonic epilepsy
Inborn genetic diseases
DOORS syndrome
Developmental and epileptic encephalopathy
1
Autosomal dominant nonsyndromic hearing loss 65
Familial infantile myoclonic epilepsy
Inborn genetic diseases
DOORS syndrome
Developmental and epileptic encephalopathy
1
Autosomal dominant nonsyndromic hearing loss 65
Other Variants in TBC1D24