ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1432+16A>G

gnomAD frequency: 0.00001  dbSNP: rs753631065
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409517 SCV000488596 uncertain significance Paragangliomas 5 2016-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058840 SCV002456298 likely benign Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2024-01-10 criteria provided, single submitter clinical testing

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.