List of variants in gene GLDC reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.319A>G (p.Met107Val)	rs138454333	0.00707
NM_000170.3(GLDC):c.52G>T (p.Gly18Cys)	rs535143891	0.00670
NM_000170.3(GLDC):c.1229G>A (p.Arg410Lys)	rs144090917	0.00234
NM_000170.3(GLDC):c.498T>C (p.Pro166=)	rs150193069	0.00110
NM_000170.3(GLDC):c.2730G>A (p.Ser910=)	rs144937031	0.00061
NM_000170.3(GLDC):c.2181C>T (p.Asp727=)	rs192045547	0.00005
NM_000170.3(GLDC):c.2310C>A (p.Ile770=)	rs765661419

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