List of variants reported as likely benign for Tyrosinase-positive oculocutaneous albinism

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000275.3(OCA2):c.796C>T (p.Arg266Trp)	rs33929465	0.00876
NM_000275.3(OCA2):c.574-19A>G	rs145242923	0.00618
NM_000275.3(OCA2):c.1679G>A (p.Arg560His)	rs35110389	0.00395
NM_000275.3(OCA2):c.126C>T (p.Ala42=)	rs141135991	0.00362
NM_000275.3(OCA2):c.1744C>T (p.Leu582=)	rs61751032	0.00302
NM_000275.3(OCA2):c.1560C>A (p.Leu520=)	rs140932222	0.00176
NM_000275.3(OCA2):c.1857C>T (p.Asp619=)	rs7164127	0.00070
NM_000275.3(OCA2):c.1762C>T (p.Arg588Trp)	rs150711896	0.00045
NM_000275.3(OCA2):c.*271G>A	rs151210258	0.00042
NM_000275.3(OCA2):c.45G>A (p.Pro15=)	rs202091837	0.00028
NM_000275.3(OCA2):c.144G>A (p.Ser48=)	rs374819923	0.00026
NM_000275.3(OCA2):c.1160C>T (p.Thr387Met)	rs150335311	0.00019
NM_000275.3(OCA2):c.1785-7C>G	rs375281082	0.00011
NM_000275.3(OCA2):c.1479T>G (p.Val493=)	rs374434751	0.00009
NM_000275.3(OCA2):c.2245-6C>A	rs368772032	0.00009
NM_000275.3(OCA2):c.2432+11A>G	rs145577954	0.00009
NM_000275.3(OCA2):c.2043C>G (p.Thr681=)	rs368126732	0.00006
NM_000275.3(OCA2):c.2208G>T (p.Ser736=)	rs1800418

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