ClinVar Miner

List of variants reported as benign for Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome; 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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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.1326C>T (p.Tyr442=)	rs184639841	0.00324

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