ClinVar Miner

List of variants in gene SDHC reported as likely pathogenic for Hereditary Paraganglioma-Pheochromocytoma Syndromes

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_003001.3(SDHC):c.21-3_22del rs1553261757
NM_003001.3(SDHC):c.405+1G>A rs587776653
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys) rs587778661

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.