ClinVar Miner

List of variants in gene SCO2 reported as uncertain significance for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_001169109.1(SCO2):c.-14+505G>A rs375309432
NM_001169109.1(SCO2):c.-14+646G>C rs145052206
NM_001169109.1(SCO2):c.-14+674G>C rs554814235
NM_001169109.1(SCO2):c.-14+705A>G rs886057632
NM_001169109.1(SCO2):c.-14+737C>T rs886057631

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.