C0574080[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 21068	NM_000156.6(GAMT):c.626C>T (p.Thr209Met)	GAMT, NDUFS7 (T209M)	Single nucleotide variant (missense variant)	Deficiency of guanidinoacetate methyltransferase	GBenign FDA Recognized database
Select item 21067	NM_000156.6(GAMT):c.460-31G>A	GAMT	Single nucleotide variant (intron variant)	Deficiency of guanidinoacetate methyltransferase +2 more	GBenign
Select item 1184667	NM_000156.6(GAMT):c.391+47A>G	GAMT	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

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