C1847626[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4103	NM_138691.3(TMC1):c.100C>T (p.Arg34Ter)	TMC1 (R34*)	Single nucleotide variant (nonsense)	Autosomal dominant nonsyndromic hearing loss 36 +3 more	GPathogenic
Select item 1333340	NM_138691.3(TMC1):c.1975C>A (p.Pro659Thr)	TMC1 (P659T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 36	GUncertain significance