List of variants reported as likely benign for Very long chain acyl-CoA dehydrogenase deficiency by ClinGen ACADVL Variant Curation Expert Panel, ClinGen

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln)	rs148584617	0.00244
NM_000018.4(ACADVL):c.663C>T (p.Ser221=)	rs144255994	0.00116
NM_000018.4(ACADVL):c.1077+15C>T	rs202237278	0.00041
NM_000018.4(ACADVL):c.822C>T (p.Ala274=)	rs372038260	0.00002
NM_000018.4(ACADVL):c.117C>T (p.Pro39=)	rs370883584	0.00001
NM_000018.4(ACADVL):c.1533G>A (p.Arg511=)	rs886038214
NM_000018.4(ACADVL):c.189A>G (p.Lys63=)	rs727503790
NM_000018.4(ACADVL):c.579C>T (p.Gly193=)
NM_000018.4(ACADVL):c.96G>A (p.Arg32=)	rs1243371051

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