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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1839G>A (p.Arg613=)	rs79125791	0.00254
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln)	rs148584617	0.00244
NM_000018.4(ACADVL):c.1828-4C>G	rs184559206	0.00192
NM_000018.4(ACADVL):c.1473A>G (p.Leu491=)	rs150518187	0.00051
NM_000018.4(ACADVL):c.1077+15C>T	rs202237278	0.00041
NM_000018.4(ACADVL):c.1533-4T>A	rs369986567	0.00026
NM_000018.4(ACADVL):c.*8C>T	rs370513576	0.00011
NM_000018.4(ACADVL):c.114G>C (p.Arg38=)	rs777380964	0.00009
NM_000018.4(ACADVL):c.264C>T (p.Phe88=)	rs147357106	0.00006
NM_000018.4(ACADVL):c.255T>C (p.Asp85=)	rs201085520	0.00004
NM_000018.4(ACADVL):c.963C>T (p.Asn321=)	rs568118142	0.00002
NM_000018.4(ACADVL):c.117C>T (p.Pro39=)	rs370883584	0.00001
NM_000018.4(ACADVL):c.1494T>G (p.Ala498=)	rs756867868	0.00001
NM_000018.4(ACADVL):c.1575C>A (p.Val525=)	rs745996278	0.00001
NM_000018.4(ACADVL):c.1605+7G>C	rs572010910

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.