List of variants in gene combination CHAT, SLC18A3 reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003055.3(SLC18A3):c.347del (p.Pro116fs)	rs1554800550
NM_003055.3(SLC18A3):c.599T>A (p.Ile200Asn)	rs1554800621
NM_003055.3(SLC18A3):c.945G>A (p.Trp315Ter)	rs1554800734

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