List of variants in gene NARS2 reported as benign for nonsyndromic genetic hearing loss

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024678.6(NARS2):c.260A>C (p.Asn87Thr)	rs10501429	0.76474
NM_024678.6(NARS2):c.414T>C (p.Tyr138=)	rs10751296	0.71183

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