List of variants reported as likely pathogenic for Hyperornithinemia

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000274.4(OAT):c.722C>T (p.Pro241Leu)	rs121965051	0.00001
NM_000274.4(OAT):c.461G>T (p.Arg154Leu)	rs121965039
NM_000274.4(OAT):c.583G>T (p.Asp195Tyr)	rs386833614
NM_000274.4(OAT):c.881_900+51del	rs1951451290

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