List of variants in gene TRRAP reported as benign for autosomal dominant nonsyndromic hearing loss

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_001375524.1(TRRAP):c.2200-46C>T	rs1859662	0.69438
NM_001375524.1(TRRAP):c.898-46C>T	rs7777927	0.69053

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