List of variants in gene combination HMGCS2, PHGDH reported as likely benign for inborn disorder of amino acid metabolism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006623.3(PHGDH):c.*200A>G	rs17258425	0.11740
NM_005518.4(HMGCS2):c.*332A>C	rs56828380	0.02618
NM_005518.4(HMGCS2):c.*165C>T	rs138575225	0.01059

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