List of variants in gene ESRRB 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001379180.1(ESRRB):c.948T>C (p.Tyr316=)	rs2361293	0.99538
NM_001379180.1(ESRRB):c.*2906T>C	rs3829784	0.43496
NM_001379180.1(ESRRB):c.*2504T>C	rs3813545	0.23239
NM_001379180.1(ESRRB):c.144C>A (p.Ile48=)	rs35544003	0.07261
NM_001379180.1(ESRRB):c.1219C>T (p.Pro407Ser)	rs61742642	0.06008
NM_001379180.1(ESRRB):c.79A>G (p.Arg27Gly)	rs143477571	0.00137
NM_001379180.1(ESRRB):c.*2574C>A	rs8017684

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