List of variants in gene LMX1A reported as likely pathogenic for autosomal dominant nonsyndromic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_177398.4(LMX1A):c.331del (p.Gln111fs)	rs2102637875
NM_177398.4(LMX1A):c.596G>A (p.Arg199Lys)
NM_177398.4(LMX1A):c.937C>T (p.Arg313Ter)

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