C1863688[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065846	NM_017947.4(MOCOS):c.2271-1G>A	MOCOS	Single nucleotide variant (splice acceptor variant)	Xanthinuria type II	GLikely pathogenic
Select item 253162	NM_017947.4(MOCOS):c.2326C>T (p.Arg776Cys)	MOCOS (R776C)	Single nucleotide variant (missense variant)	Xanthinuria type II	GLikely pathogenic