List of variants in gene STRC reported as uncertain significance 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.4918C>T (p.Leu1640Phe)	rs2920791	0.00174
NM_153700.2(STRC):c.3218G>A (p.Arg1073Gln)	rs727503449	0.00085
NM_153700.2(STRC):c.3307-5T>G	rs727503446	0.00014
NM_153700.2(STRC):c.3275G>A (p.Cys1092Tyr)	rs727503447	0.00005
NM_153700.2(STRC):c.1576C>T (p.Arg526Cys)	rs1555447608
NM_153700.2(STRC):c.2303_2313+1del	rs1021413948
NM_153700.2(STRC):c.274C>T (p.Arg92Trp)	rs1484849703
NM_153700.2(STRC):c.3091C>A (p.Pro1031Thr)	rs1595961729
NM_153700.2(STRC):c.4765G>T (p.Val1589Phe)	rs147963245
NM_153700.2(STRC):c.4917_4918delinsCT (p.Leu1640Phe)	rs727503441

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