List of variants in gene TBC1D24 reported as uncertain significance for DOORS syndrome; Familial infantile myoclonic epilepsy; Autosomal recessive nonsyndromic hearing loss 86; Developmental and epileptic encephalopathy, 16; Autosomal dominant nonsyndromic hearing loss 65

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.1327G>A (p.Glu443Lys)	rs141399869	0.00163
NM_001199107.2(TBC1D24):c.871G>A (p.Ala291Thr)	rs375307187	0.00011
NM_001199107.2(TBC1D24):c.734T>C (p.Leu245Pro)	rs370477379	0.00001

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