C0086795[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1526094	NM_000203.5(IDUA):c.589G>A (p.Gly197Ser)	IDUA (G197S +1 more)	Single nucleotide variant (missense variant +1 more)	Hurler syndrome	GLikely pathogenic
Select item 1526193	NM_000203.5(IDUA):c.589+1G>T	IDUA	Single nucleotide variant (splice donor variant)	Hurler syndrome	GLikely pathogenic
Select item 11919	NM_000203.5(IDUA):c.1469T>C (p.Leu490Pro)	IDUA (L490P +1 more)	Single nucleotide variant (missense variant +1 more)	Hurler syndrome +2 more	GPathogenic/Likely pathogenic

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