C2675179[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 129137	NM_001482.3(GATM):c.1252T>C (p.Leu418=)	GATM	Single nucleotide variant (synonymous variant)	Arginine:glycine amidinotransferase deficiency	GBenign FDA Recognized database
Select item 129138	NM_001482.3(GATM):c.330A>T (p.Gln110His)	GATM (Q110H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +4 more	GBenign/Likely benign