Variants in gene G6PC1 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000151.4(G6PC1):c.14T>G (p.Met5Arg)	rs1250172816	0.00002
NM_000151.4(G6PC1):c.326G>A (p.Cys109Tyr)	rs886052955	0.00001
NM_000151.4(G6PC1):c.500G>A (p.Cys167Tyr)	rs777552825	0.00001
NM_000151.4(G6PC1):c.706T>A (p.Trp236Arg)	rs2056092151
NM_000151.4(G6PC1):c.792C>A (p.Asn264Lys)	rs1555560149
NM_000151.4(G6PC1):c.964T>G (p.Phe322Val)	rs1567706564
NM_000151.4(G6PC1):c.965T>A (p.Phe322Tyr)	rs863224022

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