List of variants in gene ESRRB reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001379180.1(ESRRB):c.1219C>T (p.Pro407Ser)	rs61742642	0.06008
NM_001379180.1(ESRRB):c.204G>C (p.Leu68=)	rs61744548	0.01800
NM_001379180.1(ESRRB):c.1300G>A (p.Val434Ile)	rs146351534	0.01096
NM_001379180.1(ESRRB):c.*1474T>C	rs188462546	0.00354

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