List of variants in gene TYR reported as likely benign for disorder of melanin metabolism

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1205G>A (p.Arg402Gln)	rs1126809	0.18094
NM_000372.5(TYR):c.835T>C (p.Leu279=)	rs4987234	0.00733
NM_000372.5(TYR):c.665T>C (p.Ile222Thr)	rs34878847	0.00096
NM_000372.5(TYR):c.504C>T (p.Asn168=)	rs148813091	0.00051
NM_000372.5(TYR):c.573A>G (p.Gly191=)	rs372123800	0.00016
NM_000372.5(TYR):c.48C>T (p.Ser16=)	rs148710429	0.00006
NM_000372.5(TYR):c.1036+13T>A	rs1377064834

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