List of variants reported as benign for Very long chain acyl-CoA dehydrogenase deficiency by Illumina Laboratory Services, Illumina

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1605+6T>C	rs17671352	0.56622
NM_001033859.2(ACADVL):c.-63_-49dup	rs6145976	0.50677
NM_000018.4(ACADVL):c.194C>T (p.Pro65Leu)	rs28934585	0.03462
NM_000018.4(ACADVL):c.128G>A (p.Gly43Asp)	rs2230178	0.02763
NM_000018.4(ACADVL):c.1038G>A (p.Ala346=)	rs8064573	0.02419
NM_000018.4(ACADVL):c.49C>T (p.Leu17Phe)	rs2230179	0.02069
NM_000018.4(ACADVL):c.1600G>A (p.Glu534Lys)	rs2230180	0.00920
NM_000018.4(ACADVL):c.623-8C>T	rs144996066	0.00919
NM_000018.4(ACADVL):c.68G>A (p.Arg23Gln)	rs34153370	0.00034

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