List of variants in gene TYR reported as benign by Illumina Laboratory Services, Illumina

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.575C>A (p.Ser192Tyr)	rs1042602	0.24046
NM_000372.5(TYR):c.114G>A (p.Pro38=)	rs1939261	0.01433
NM_000372.5(TYR):c.178C>T (p.Leu60=)	rs1939260	0.01429

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