ClinVar Miner

List of variants in gene SDHAF2 reported as uncertain significance for benign endocrine neoplasm

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_017841.2(SDHAF2):c.*113C>A rs886048416
NM_017841.2(SDHAF2):c.*170C>A rs886048417
NM_017841.2(SDHAF2):c.*172del rs537244040
NM_017841.2(SDHAF2):c.*627G>T rs886048422
NM_017841.2(SDHAF2):c.*653A>G rs886048423
NM_017841.2(SDHAF2):c.370+12G>A rs886048415

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.