Variants in gene GAMT with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 3

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HGVS	dbSNP
NM_000156.6(GAMT):c.438A>G (p.Thr146=)	rs80338733
NM_000156.6(GAMT):c.581T>C (p.Val194Ala)	rs147739199
NM_000156.6(GAMT):c.79T>C (p.Tyr27His)	rs200833152

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