RS398122967 TBC1D24
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What This Variant Does
"CLNSIG=5
Associated Conditions
DOORS syndrome
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
Developmental and epileptic encephalopathy
16
TBC1D24-related disorder
Monogenic hearing loss
1
DOORS syndrome
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
Developmental and epileptic encephalopathy
16
TBC1D24-related disorder
Monogenic hearing loss
Other Variants in TBC1D24