List of variants in gene KCNJ10 reported as likely pathogenic for autosomal recessive nonsyndromic hearing loss 4

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys)	rs137853074	0.00008
NM_002241.5(KCNJ10):c.76C>T (p.Arg26Ter)	rs138943405	0.00001
NM_002241.5(KCNJ10):c.889C>T (p.Arg297Cys)	rs137853071

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