List of variants in gene TWNK reported as likely pathogenic for auditory system disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP
NM_021830.5(TWNK):c.737A>G (p.Asn246Ser)	rs754081544

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