"GATM-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137451	NM_001482.3(GATM):c.1239G>A (p.Arg413=)	GATM	Single nucleotide variant (synonymous variant)	Arginine:glycine amidinotransferase deficiency	GBenign FDA Recognized database
Select item 2632315	NM_001482.3(GATM):c.1183A>G (p.Ile395Val)	GATM (I266V +1 more)	Single nucleotide variant (missense variant)	GATM-related disorder	GUncertain significance
Select item 205618	NM_001482.3(GATM):c.1105C>T (p.Arg369Cys)	GATM (R369C +1 more)	Single nucleotide variant (missense variant)	Arginine:glycine amidinotransferase deficiency +2 more	GUncertain significance
Select item 2632421	NM_001482.3(GATM):c.834T>G (p.Ile278Met)	GATM (I149M +1 more)	Single nucleotide variant (missense variant)	GATM-related disorder	GUncertain significance
Select item 1054800	NM_001482.3(GATM):c.675+9C>G	GATM	Single nucleotide variant (intron variant)	GATM-related disorder +1 more	GLikely benign
Select item 2632252	NM_001482.3(GATM):c.595A>G (p.Ile199Val)	GATM (I199V +1 more)	Single nucleotide variant (missense variant)	GATM-related disorder +1 more	GUncertain significance
Select item 377914	NM_001482.3(GATM):c.-9G>T	GATM, LOC130056991	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign

ClinVar