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

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.*2040C>G	rs2486254	0.99734
NM_002241.5(KCNJ10):c.*2062T>G	rs1053074	0.45911
NM_002241.5(KCNJ10):c.*1764T>G	rs2486253

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