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

Submission 1 (pathogenic) minimum review status:		Submission 1 (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: 2

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HGVS	dbSNP
NM_000030.3(AGXT):c.822G>C (p.Glu274Asp)	rs146525143
NM_000030.3(AGXT):c.866G>A (p.Arg289His)	rs61729604

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