List of variants in gene TYRP1 reported as benign for oculocutaneous albinism

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000550.3(TYRP1):c.259C>A (p.Arg87=)	rs34509359	0.04615
NM_000550.3(TYRP1):c.729T>C (p.Ser243=)	rs35866166	0.04447
NM_000550.3(TYRP1):c.-161G>T	rs7867043	0.04161
NM_000550.3(TYRP1):c.98T>C (p.Val33Ala)	rs146838872	0.00128

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