List of variants in gene TYR reported as benign by PreventionGenetics, part of Exact Sciences

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.178C>T (p.Leu60=)	rs1939260	0.01429
NM_000372.5(TYR):c.504C>T (p.Asn168=)	rs148813091	0.00051
NM_000372.5(TYR):c.1037-21dup	rs3834913

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