List of variants in gene CHAT reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020549.5(CHAT):c.-10T>G	rs7923716	0.97663
NM_020549.5(CHAT):c.1641T>C (p.His547=)	rs8178992	0.82309
NM_020549.5(CHAT):c.358G>A (p.Ala120Thr)	rs3810950	0.17408
NM_020549.5(CHAT):c.287-431G>A	rs1880676	0.17399
NM_020549.5(CHAT):c.727C>T (p.Leu243Phe)	rs8178990	0.04717
NM_020549.5(CHAT):c.1381G>A (p.Val461Met)	rs4838544

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