"SLC18A2-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 742989	NM_003054.6(SLC18A2):c.147C>T (p.Tyr49=)	SLC18A2	Single nucleotide variant (synonymous variant)	SLC18A2-related disorder +1 more	GLikely benign
Select item 717979	NM_003054.6(SLC18A2):c.203C>T (p.Thr68Ile)	SLC18A2 (T68I)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 791308	NM_003054.6(SLC18A2):c.255G>A (p.Ser85=)	SLC18A2	Single nucleotide variant (synonymous variant)	SLC18A2-related disorder +1 more	GLikely benign
Select item 1168452	NM_003054.6(SLC18A2):c.597C>T (p.Ser199=)	SLC18A2	Single nucleotide variant (synonymous variant)	SLC18A2-related disorder +1 more	GBenign
Select item 1557598	NM_003054.6(SLC18A2):c.835-7T>G	SLC18A2	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1458309	NM_003054.6(SLC18A2):c.1544GAGAT[1] (p.Ter515=)	SLC18A2	Microsatellite (no sequence alteration)	not provided +1 more	GLikely benign

ClinVar