List of variants in gene TYR reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.665T>C (p.Ile222Thr)	rs34878847	0.00096
NM_000372.5(TYR):c.1509G>C (p.Lys503Asn)	rs138750983	0.00052
NM_000372.5(TYR):c.454C>T (p.Pro152Ser)	rs145513733	0.00024
NM_000372.5(TYR):c.26T>C (p.Leu9Pro)	rs1238837002	0.00001
NM_000372.5(TYR):c.841G>A (p.Glu281Lys)	rs142629239

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