ClinVar Miner

List of variants in gene combination DHCR7, NADSYN1 reported as uncertain significance for Smith-Lemli-Opitz syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
Download table as spreadsheet
NM_001360.2(DHCR7):c.376G>A (p.Val126Ile) rs143587828

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.