List of variants in gene SAG reported as benign for inborn disorder of amino acid metabolism

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000541.5(SAG):c.1207G>A (p.Val403Ile)	rs1046974	0.30851
NM_000541.5(SAG):c.489C>T (p.Ala163=)	rs2304773	0.13074
NM_000541.5(SAG):c.1208T>C (p.Val403Ala)	rs1046976	0.12771
NM_000541.5(SAG):c.226A>G (p.Ile76Val)	rs7565275	0.06304
NM_000541.5(SAG):c.1047-13T>C	rs73995909	0.03685
NM_000541.5(SAG):c.321G>C (p.Leu107=)	rs59676190	0.03222
NM_000541.5(SAG):c.*7C>T	rs692	0.02006
NM_000541.5(SAG):c.93G>A (p.Gly31=)	rs79063407	0.00807

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