List of variants reported as likely pathogenic for Tyrosinase-negative oculocutaneous albinism; Oculocutaneous albinism type 1B

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.121G>A (p.Gly41Arg)	rs369291837	0.00002
NM_000372.5(TYR):c.551C>G (p.Ser184Ter)	rs367543066	0.00001
NM_000372.5(TYR):c.1037G>A (p.Gly346Glu)	rs773970123
NM_000372.5(TYR):c.1045_1046insAT (p.Ser349fs)
NM_000372.5(TYR):c.1109T>A (p.Met370Lys)
NM_000372.5(TYR):c.635G>C (p.Arg212Thr)

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