List of variants in gene KARS1 reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 89

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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_005548.3(KARS1):c.797T>C (p.Ile266Thr)	rs762673443	0.00003
NM_005548.3(KARS1):c.787T>G (p.Phe263Val)	rs772410450	0.00001
NM_005548.3(KARS1):c.1513C>G (p.Pro505Ala)	rs1555512658

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