List of variants reported as benign for Very long chain acyl-CoA dehydrogenase deficiency by Natera, Inc.

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1605+6T>C	rs17671352	0.56622
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.636C>T (p.Ala212=)	rs76547988	0.00560
NM_000018.4(ACADVL):c.308A>G (p.Lys103Arg)	rs140566084	0.00391
NM_000018.4(ACADVL):c.1824C>T (p.Ile608=)	rs146115467	0.00058
NM_000018.4(ACADVL):c.693T>A (p.Ser231=)	rs77763289

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