List of variants reported as uncertain significance for inborn disorder of amino acid metabolism by Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS)

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_016335.6(PRODH):c.1322T>C (p.Leu441Pro)	rs2904551	0.00282
NM_003124.5(SPR):c.370T>C (p.Trp124Arg)
NM_022132.5(MCCC2):c.281+5G>T

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