List of variants in gene TMC1 reported as likely pathogenic for obsolete rare genetic deafness

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_138691.3(TMC1):c.1333C>T (p.Arg445Cys)	rs372710475	0.00005
NM_138691.3(TMC1):c.1141T>A (p.Tyr381Asn)	rs749491943	0.00003
NM_138691.3(TMC1):c.674C>T (p.Pro225Leu)	rs370088722	0.00002
NM_138691.3(TMC1):c.741+1G>A	rs1588067173

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