List of variants in gene TYR reported as likely benign for not specified

Minimum submission review status:		Collection method:
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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	0.24046
NM_000372.5(TYR):c.1205G>A (p.Arg402Gln)	rs1126809	0.17677
NM_000372.5(TYR):c.114G>A (p.Pro38=)	rs1939261	0.01433
NM_000372.5(TYR):c.835T>C (p.Leu279=)	rs4987234	0.00733
NM_000372.5(TYR):c.-10T>C	rs368061096	0.00002

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