ClinVar Miner

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

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
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.693T>A (p.Ser231=)	rs77763289

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