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

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_021830.5(TWNK):c.1217G>A (p.Arg406Gln)	rs756073260	0.00001
NM_021830.5(TWNK):c.1388G>A (p.Arg463Gln)	rs757583061	0.00001

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