RS141399869 TBC1D24
Upload your DNA to see your genotype for this variant.
Associated Conditions
DOORS syndrome
Developmental and epileptic encephalopathy
16
Familial infantile myoclonic epilepsy
Autosomal recessive nonsyndromic hearing loss 86
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
1
DOORS syndrome
Developmental and epileptic encephalopathy
16
Familial infantile myoclonic epilepsy
Autosomal recessive nonsyndromic hearing loss 86
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
Other Variants in TBC1D24