List of variants in gene combination SMIM27, TOPORS reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005802.5(TOPORS):c.-64C>T	rs776476617	0.00001
NM_005802.5(TOPORS):c.3+3A>G	rs2040734643	0.00001

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