List of variants in gene REST reported as likely 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_005612.5(REST):c.898+15C>T	rs148949163	0.00026
NM_005612.5(REST):c.3098A>G (p.His1033Arg)	rs572949989

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