List of variants in gene SLC18A2 reported as uncertain significance for Brain dopamine-serotonin vesicular transport disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003054.6(SLC18A2):c.1196A>C (p.Asp399Ala)	rs758715677
NM_003054.6(SLC18A2):c.590C>T (p.Ser197Phe)	rs2493539476
NM_003054.6(SLC18A2):c.596C>T (p.Ser199Phe)
NM_003054.6(SLC18A2):c.710C>A (p.Pro237His)	rs767337086

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