List of variants in gene STRC reported as likely benign for autosomal recessive nonsyndromic hearing loss 16

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_153700.2(STRC):c.179T>C (p.Phe60Ser)	rs2729509	0.34286
NM_153700.2(STRC):c.3360T>C (p.Cys1120=)	rs56385906	0.01920
NM_153700.2(STRC):c.498G>A (p.Pro166=)	rs139848805	0.00486
NM_153700.2(STRC):c.5200T>C (p.Trp1734Arg)	rs200770543	0.00124
NM_153700.2(STRC):c.4917A>C (p.Leu1639=)	rs2860666	0.00112
NM_153700.2(STRC):c.3555G>A (p.Leu1185=)	rs2597064	0.00014
NM_153700.2(STRC):c.4845C>T (p.Ser1615=)	rs184909019	0.00010
NM_153700.2(STRC):c.3681+11G>A	rs796781098

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