List of variants in gene TYR reported as uncertain significance for Oculocutaneous albinism type 1A; Oculocutaneous albinism type 1B

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.1509G>C (p.Lys503Asn)	rs138750983	0.00047
NM_000372.5(TYR):c.1067A>T (p.Asp356Val)	rs180801021	0.00037
NM_000372.5(TYR):c.1352A>G (p.Tyr451Cys)	rs376823382	0.00023
NM_000372.5(TYR):c.1132C>A (p.Gln378Lys)

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