List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 35 by Illumina Laboratory Services, Illumina

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Total variants: 6

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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.79A>G (p.Arg27Gly)	rs143477571	0.00137
NM_001379180.1(ESRRB):c.*2574C>A	rs8017684

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