List of variants in gene TMC6 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127198.5(TMC6):c.1505C>T (p.Pro502Leu)	rs75400929	0.00763
NM_001127198.5(TMC6):c.1536-4G>A	rs117553598	0.00265
NM_001127198.5(TMC6):c.1842C>T (p.Pro614=)	rs150820026	0.00055
NM_001127198.5(TMC6):c.1914G>A (p.Ala638=)
NM_001127198.5(TMC6):c.1980C>T (p.Ala660=)	rs1019287801

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