List of variants in gene GLDC reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.2053-5C>G	rs140877566	0.00278
NM_000170.3(GLDC):c.1750C>T (p.Pro584Ser)	rs1001664445	0.00002
NM_000170.3(GLDC):c.2791G>A (p.Ala931Thr)	rs1057520185

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