List of variants in gene combination GPHN, RDH12 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152443.3(RDH12):c.-275+12C>T	rs73276636	0.03015
NM_152443.3(RDH12):c.-152A>G	rs76635633	0.00699
NM_152443.3(RDH12):c.570C>T (p.Ser190=)	rs79869437	0.00041

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