ClinVar for PubMed (Select 1703535) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2681193	NM_000030.3(AGXT):c.[32C>T;836T>C]	AGXT (P11L +1 more)	Single nucleotide variant (missense variant)	Primary hyperoxaluria, type I	GPathogenic
Select item 40166	NM_000030.3(AGXT):c.508G>A (p.Gly170Arg)	AGXT (G170R)	Single nucleotide variant (missense variant)	AGXT-related condition +3 more	GPathogenic/Likely pathogenic
Select item 5641	NM_000030.3(AGXT):c.32C>T (p.Pro11Leu)	AGXT (P11L)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign

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