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

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.478-106del	rs370388543	0.60962
NM_000018.4(ACADVL):c.1605+6T>C	rs17671352	0.56622
NM_000018.4(ACADVL):c.478-22_478-21del	rs60400822	0.07027
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.623-8C>T	rs144996066	0.00919
NM_000018.4(ACADVL):c.636C>T (p.Ala212=)	rs76547988	0.00560
NM_000018.3(ACADVL):c.-64T>C	rs77051465	0.00545
NM_000018.4(ACADVL):c.879-50G>T	rs11870841	0.00481
NM_000018.4(ACADVL):c.63-35G>A	rs774905326	0.00053
NM_000018.4(ACADVL):c.68G>A (p.Arg23Gln)	rs34153370	0.00034
NM_000018.4(ACADVL):c.693T>A (p.Ser231=)	rs77763289

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