List of variants reported as likely benign for Coenzyme Q10 deficiency, primary, 3 by Fulgent Genetics, Fulgent Genetics

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020381.4(PDSS2):c.431+17C>T	rs192411971	0.00141
NM_020381.4(PDSS2):c.1009-14C>G	rs188095740	0.00084
NM_020381.4(PDSS2):c.877-20C>T	rs138097933	0.00043
NM_020381.4(PDSS2):c.702+16G>A	rs200017192	0.00012
NM_020381.4(PDSS2):c.81G>A (p.Pro27=)	rs754281828	0.00010
NM_020381.4(PDSS2):c.1002C>T (p.Ile334=)	rs375546963	0.00006
NM_020381.4(PDSS2):c.1008+17C>T	rs760414222	0.00006
NM_020381.4(PDSS2):c.348G>T (p.Val116=)	rs779485875	0.00002
NM_020381.4(PDSS2):c.1134C>T (p.Ser378=)	rs543231659

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.