RS397514713 TBC1D24

Health Risk Chr 16:2496834
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
16
Caused by mutation in the TBC1 domain family
member 24
Autosomal dominant nonsyndromic hearing loss 65
1
Developmental and epileptic encephalopathy
16
Caused by mutation in the TBC1 domain family
member 24
Autosomal dominant nonsyndromic hearing loss 65
1
Other Variants in TBC1D24
rs267607103 rs267607105 rs267607104 rs398122941 rs397514714 rs398122965 rs398122966 rs201257588 rs398122967 rs398122968
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