ClinVar Miner

List of variants in gene CHAT reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020549.5(CHAT):c.1682G>A (p.Arg561Gln)	rs80097077	0.00825
NM_020549.5(CHAT):c.896C>T (p.Pro299Leu)	rs868749	0.00385

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