Variants in gene GLDC with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 23

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.2852C>A (p.Ser951Tyr)	rs147472391	0.00036
NM_000170.3(GLDC):c.2607C>A (p.Pro869=)	rs386833565	0.00009
NM_000170.3(GLDC):c.1940C>T (p.Pro647Leu)	rs201135624	0.00006
NM_000170.3(GLDC):c.1033C>A (p.Pro345Thr)	rs373263202	0.00001
NM_000170.3(GLDC):c.1078G>C (p.Val360Leu)	rs373482451	0.00001
NM_000170.3(GLDC):c.1117C>T (p.Arg373Trp)	rs150171524	0.00001
NM_000170.3(GLDC):c.1381C>T (p.Arg461Trp)	rs761957837	0.00001
NM_000170.3(GLDC):c.1606C>T (p.Arg536Trp)	rs1286882965	0.00001
NM_000170.3(GLDC):c.2368C>T (p.Arg790Trp)	rs386833556	0.00001
NM_000170.3(GLDC):c.2963G>A (p.Arg988Gln)	rs749512886	0.00001
NM_000170.3(GLDC):c.799C>G (p.Pro267Ala)	rs1554648117	0.00001
NM_000170.3(GLDC):c.800C>T (p.Pro267Leu)	rs138484426	0.00001
NM_000170.3(GLDC):c.1084C>T (p.Arg362Cys)	rs10975674
NM_000170.3(GLDC):c.1183T>C (p.Phe395Leu)	rs767200188
NM_000170.3(GLDC):c.1654A>G (p.Met552Val)	rs386833529
NM_000170.3(GLDC):c.1738C>G (p.His580Asp)	rs1164241828
NM_000170.3(GLDC):c.1970G>A (p.Ser657Asn)	rs1301895668
NM_000170.3(GLDC):c.2238T>A (p.Asp746Glu)	rs749882600
NM_000170.3(GLDC):c.245T>C (p.Leu82Ser)	rs386833559
NM_000170.3(GLDC):c.2578G>C (p.Gly860Arg)	rs753759723
NM_000170.3(GLDC):c.2729C>T (p.Ser910Leu)	rs759933539
NM_000170.3(GLDC):c.2798T>C (p.Ile933Thr)	rs758029533
NM_000170.3(GLDC):c.2962C>T (p.Arg988Trp)	rs1288008254

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