List of variants in gene STRC reported as benign for auditory system disorder

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: 10

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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.4842C>T (p.Phe1614=)	rs3097773	0.29444
NM_153700.2(STRC):c.4878C>G (p.Leu1626=)	rs12438025	0.22424
NM_153700.2(STRC):c.4845-13T>C	rs12437957	0.22423
NM_153700.2(STRC):c.3893A>G (p.His1298Arg)	rs2920780	0.22075
NM_153700.2(STRC):c.3702G>A (p.Glu1234=)	rs62018890	0.15683
NM_153700.2(STRC):c.4035G>C (p.Leu1345=)	rs143345370	0.01824
NM_153700.2(STRC):c.4127+8C>T	rs2470137	0.01144
NM_153700.2(STRC):c.3540T>G (p.Leu1180=)	rs199524735	0.00335
NM_153700.2(STRC):c.22CTG[10] (p.Leu18del)	rs1567120678

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