List of variants in gene DPAGT1 reported as uncertain significance by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001382.4(DPAGT1):c.1201C>T (p.Leu401Phe)	rs150532554	0.00016
NM_001382.4(DPAGT1):c.1154T>G (p.Leu385Arg)	rs1016844949	0.00007
NM_001382.4(DPAGT1):c.584C>G (p.Ala195Gly)	rs863225088	0.00001
NM_001382.4(DPAGT1):c.304C>T (p.Leu102Phe)

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