List of variants reported as likely pathogenic for oculocutaneous albinism type 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000275.3(OCA2):c.1503+5G>A	rs368124046	0.00008
NM_000275.3(OCA2):c.2360C>T (p.Ala787Val)	rs200457227	0.00004
NM_000275.3(OCA2):c.2330G>A (p.Cys777Tyr)	rs776814755	0.00001
NM_000275.3(OCA2):c.807+1G>T	rs763219039	0.00001
NM_000275.3(OCA2):c.868A>G (p.Arg290Gly)	rs769408559	0.00001
NM_000275.3(OCA2):c.619_636del (p.Leu207_Leu212del)	rs767489236

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