List of variants in gene TYR reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1202T>C (p.Leu401Pro)	rs2135324201
NM_000372.5(TYR):c.1234C>G (p.Pro412Ala)	rs797046081
NM_000372.5(TYR):c.157G>C (p.Gly53Arg)	rs1591133731
NM_000372.5(TYR):c.819G>A (p.Gln273=)

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