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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000030.3(AGXT):c.822G>C (p.Glu274Asp)	rs146525143	0.00007
NM_000030.3(AGXT):c.167T>A (p.Ile56Asn)	rs180177180	0.00006
NM_000030.3(AGXT):c.352C>T (p.Arg118Cys)	rs376844297	0.00006
NM_000030.3(AGXT):c.497T>C (p.Leu166Pro)	rs180177230	0.00001
NM_000030.3(AGXT):c.1110_1111del (p.Asn372fs)	rs796052075
NM_000030.3(AGXT):c.32C>G (p.Pro11Arg)	rs34116584

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