List of variants in gene TYR reported as benign for hereditary skin disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.575C>A (p.Ser192Tyr)	rs1042602	0.24593
NM_000372.5(TYR):c.1205G>A (p.Arg402Gln)	rs1126809	0.18094
NM_000372.4(TYR):c.-199C>A	rs1799989	0.16584
NM_000372.5(TYR):c.114G>A (p.Pro38=)	rs1939261	0.01561
NM_000372.5(TYR):c.178C>T (p.Leu60=)	rs1939260	0.01556

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