List of variants in gene GLDC reported as uncertain significance by Athena Diagnostics Inc

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.2683A>G (p.Met895Val)	rs141152043	0.00200
NM_000170.3(GLDC):c.1618A>C (p.Lys540Gln)	rs140516872	0.00127
NM_000170.3(GLDC):c.2852C>A (p.Ser951Tyr)	rs147472391	0.00036
NM_000170.3(GLDC):c.619C>G (p.Leu207Val)	rs142181803	0.00027
NM_000170.3(GLDC):c.2352C>T (p.Pro784=)	rs367781728	0.00017
NM_000170.3(GLDC):c.578A>G (p.Asn193Ser)	rs555919940	0.00007
NM_000170.3(GLDC):c.869C>T (p.Ala290Val)	rs534936420	0.00004
NM_000170.3(GLDC):c.1420G>A (p.Glu474Lys)	rs1554646962
NM_000170.3(GLDC):c.1791G>T (p.Glu597Asp)	rs141875337
NM_000170.3(GLDC):c.1831G>C (p.Val611Leu)	rs1554646513
NM_000170.3(GLDC):c.2876A>G (p.His959Arg)	rs572523552

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