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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.1705G>A (p.Ala569Thr)	rs151268759	0.00419
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.445C>T (p.Arg149Trp)	rs183024300	0.00002
NM_000170.3(GLDC):c.1117C>T (p.Arg373Trp)	rs150171524	0.00001
NM_000170.3(GLDC):c.1664T>G (p.Leu555Arg)	rs765384489	0.00001
NM_000170.3(GLDC):c.2196T>A (p.Asn732Lys)	rs386833544	0.00001
NM_000170.3(GLDC):c.2368C>T (p.Arg790Trp)	rs386833556	0.00001
NM_000170.3(GLDC):c.2869T>C (p.Ser957Pro)	rs386833571	0.00001
NM_000170.3(GLDC):c.2938A>G (p.Asn980Asp)	rs772574530	0.00001
NM_000170.3(GLDC):c.1595C>G (p.Thr532Arg)	rs386833527
NM_000170.3(GLDC):c.1654A>G (p.Met552Val)	rs386833529
NM_000170.3(GLDC):c.1676C>A (p.Thr559Asn)	rs1554646634
NM_000170.3(GLDC):c.1832T>G (p.Val611Gly)	rs386833533
NM_000170.3(GLDC):c.1926+5G>A	rs1554644678
NM_000170.3(GLDC):c.2033_2035del (p.Ala678del)	rs769625871
NM_000170.3(GLDC):c.2259C>G (p.His753Gln)	rs2129719894
NM_000170.3(GLDC):c.2293C>T (p.Pro765Ser)	rs386833551
NM_000170.3(GLDC):c.2297G>T (p.Gly766Val)	rs750384225
NM_000170.3(GLDC):c.2519T>A (p.Met840Lys)	rs386833561
NM_000170.3(GLDC):c.2521G>C (p.Ala841Pro)	rs386833562
NM_000170.3(GLDC):c.2631_2639del (p.Glu877_Val879del)	rs1554642294
NM_000170.3(GLDC):c.2983G>A (p.Asp995Asn)	rs1554641505
NM_000170.3(GLDC):c.560C>G (p.Thr187Arg)	rs386833582
NM_000170.3(GLDC):c.635G>A (p.Arg212Lys)	rs386833584

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