List of variants reported as benign for Deficiency of hydroxymethylglutaryl-CoA lyase by Genome-Nilou Lab

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000191.3(HMGCL):c.252+34T>C	rs2076344	0.92735
NM_000191.3(HMGCL):c.654A>G (p.Leu218=)	rs719400	0.92712
NM_000191.3(HMGCL):c.877-72T>C	rs2076343	0.27156
NM_000191.3(HMGCL):c.48G>A (p.Ala16=)	rs115611440	0.00769
NM_000191.3(HMGCL):c.393A>G (p.Ser131=)	rs56218308	0.00290
NM_000191.3(HMGCL):c.497+19G>A	rs187735179	0.00172
NM_000191.3(HMGCL):c.-91G>T	rs6697805

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.