C1863655[trait identifier] AND "3billion"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 813831	NM_005422.4(TECTA):c.248C>T (p.Thr83Met)	TBCEL-TECTA, TECTA (T83M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1333509	NM_005422.4(TECTA):c.2409G>A (p.Ser803=)	LOC126861365, TBCEL-TECTA +1 more	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21	GUncertain significance
Select item 178822	NM_005422.4(TECTA):c.3769G>A (p.Gly1257Ser)	TECTA, TBCEL-TECTA (G1257S +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 236058	NM_005422.4(TECTA):c.5597C>T (p.Thr1866Met)	TBCEL-TECTA, TECTA (T1866M +1 more)	Single nucleotide variant (missense variant)	Rare genetic deafness +5 more	GConflicting classifications of pathogenicity
Select item 1705546	NM_005422.4(TECTA):c.5741C>G (p.Pro1914Arg)	TBCEL-TECTA, TECTA (P1914R +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21	GUncertain significance
Select item 1687445	NM_005422.4(TECTA):c.6103G>T (p.Glu2035Ter)	TBCEL-TECTA, TECTA (E2035* +1 more)	Single nucleotide variant (nonsense)	Autosomal recessive nonsyndromic hearing loss 21	GPathogenic

ClinVar