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	gnomAD frequency
NM_000156.6(GAMT):c.581T>C (p.Val194Ala)	rs147739199	0.00076
NM_000156.6(GAMT):c.182G>A (p.Gly61Glu)	rs77168423	0.00014
NM_000156.6(GAMT):c.298C>T (p.Arg100Trp)	rs552210450	0.00010

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