List of variants in gene MITF reported as uncertain significance for perceptual disorders

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_001354604.2(MITF):c.1031C>T (p.Pro344Leu)	rs756923654	0.00001
NM_001354604.2(MITF):c.979A>C (p.Ile327Leu)	rs2107529990

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