List of variants in gene TMC6 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001127198.5(TMC6):c.2384C>T (p.Pro795Leu)	rs140852551	0.00131
NM_001127198.5(TMC6):c.73T>C (p.Tyr25His)	rs765966901	0.00010
NM_001127198.5(TMC6):c.2354G>C (p.Arg785Thr)	rs763777731	0.00009

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