List of variants in gene combination LOC126861365, TBCEL-TECTA, TECTA reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 21

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.2781T>C (p.His927=)	rs142903119	0.00395
NM_005422.4(TECTA):c.2418G>A (p.Leu806=)	rs138185038	0.00133
NM_005422.4(TECTA):c.2657A>G (p.Asn886Ser)	rs146175803	0.00061
NM_005422.4(TECTA):c.2700G>A (p.Ser900=)	rs375406423	0.00024
NM_005422.4(TECTA):c.2827C>A (p.Leu943Met)	rs139158022	0.00022
NM_005422.4(TECTA):c.2586C>G (p.Leu862=)	rs374347076	0.00005
NM_005422.4(TECTA):c.2643C>T (p.Phe881=)	rs544376595	0.00004
NM_005422.4(TECTA):c.2409G>A (p.Ser803=)	rs778543447	0.00001
NM_005422.4(TECTA):c.2674C>A (p.Leu892Met)	rs748088048	0.00001
NM_005422.4(TECTA):c.2835G>A (p.Gln945=)	rs371290564	0.00001
NM_005422.4(TECTA):c.2876G>A (p.Arg959Gln)	rs150403193	0.00001
NM_005422.4(TECTA):c.2889C>A (p.Ala963=)	rs1946659418
NM_005422.4(TECTA):c.2900C>A (p.Ala967Glu)	rs199688655

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