RS1057519630 TBC1D24
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What This Variant Does
"CLNSIG=5
Associated Conditions
Parkinsonian disorder
Autosomal dominant epilepsy
Developmental and epileptic encephalopathy
1
Caused by mutation in the TBC1 domain family
member 24
Autosomal dominant nonsyndromic hearing loss 65
DOORS syndrome
Inborn genetic diseases
Parkinsonian disorder
Autosomal dominant epilepsy
Developmental and epileptic encephalopathy
1
Caused by mutation in the TBC1 domain family
member 24
Other Variants in TBC1D24