List of variants in gene combination LURAP1L, TYRP1 reported as likely pathogenic for Oculocutaneous albinism type 3

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000550.3(TYRP1):c.1226C>T (p.Ala409Val)	rs148248971	0.00005
NM_000550.3(TYRP1):c.1103del (p.Lys368fs)	rs387906560
NM_000550.3(TYRP1):c.1145T>C (p.Leu382Pro)	rs776174514

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