List of variants in gene combination LOC129994569, MIR3936HG, SLC22A5 reported as likely 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: 2

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HGVS	dbSNP	gnomAD frequency
NC_000005.10:g.132369654C>A	rs60978556	0.00870
NM_003060.4(SLC22A5):c.-118G>A	rs538643468	0.00702

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