List of variants reported as likely benign for Primary hyperoxaluria, type I by Clinical Biochemistry Laboratory, Health Services Laboratory

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000030.3(AGXT):c.557C>T (p.Ala186Val)	rs117195882	0.00231
NM_000030.3(AGXT):c.145A>C (p.Met49Leu)	rs74205173	0.00030
NM_000030.3(AGXT):c.742G>T (p.Ala248Ser)	rs180177260	0.00004
NM_000030.3(AGXT):c.32C>T (p.Pro11Leu)	rs34116584

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