List of variants in gene SLC18A2 reported as pathogenic for not provided

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003054.6(SLC18A2):c.216dup (p.Asp73fs)
NM_003054.6(SLC18A2):c.424C>T (p.Gln142Ter)	rs2133726005
NM_003054.6(SLC18A2):c.46_55del (p.Arg16fs)
NM_003054.6(SLC18A2):c.605del (p.Ala202fs)
NM_003054.6(SLC18A2):c.710C>A (p.Pro237His)	rs767337086

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