List of variants in gene TYR reported as pathogenic for See cases

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_000372.5(TYR):c.1037-7T>A	rs61754381	0.00051
NM_000372.5(TYR):c.230G>A (p.Arg77Gln)	rs61753185	0.00007
NM_000372.5(TYR):c.896G>A (p.Arg299His)	rs61754375	0.00007

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