List of variants in gene ESRRB reported as pathogenic for nonsyndromic genetic hearing loss

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001379180.1(ESRRB):c.1081_1087dup (p.Val363fs)
NM_001379180.1(ESRRB):c.1087G>T (p.Val363Leu)	rs121909111
NM_001379180.1(ESRRB):c.392C>T (p.Ala131Val)	rs121909110
NM_001379180.1(ESRRB):c.562G>A (p.Gly188Arg)	rs1555342141
NM_001379180.1(ESRRB):c.608G>A (p.Arg203His)	rs1060499794
NM_001379180.1(ESRRB):c.850G>A (p.Gly284Ser)	rs375916159

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