ClinVar Miner

Variants with conflicting interpretations "drug response" and "uncertain risk allele"

Submission 1 (drug response) minimum review status: Submission 1 (drug response) method:
Submission 2 (uncertain risk allele) minimum review status: Submission 2 (uncertain risk allele) method:
ClinVar version:

Total variants with conflicting interpretations: 1

HGVS dbSNP gnomAD frequency
NM_000754.4(COMT):c.408C>G (p.Leu136=) rs4818 0.32165

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.