ClinVar Miner

List of variants in gene ATP7B reported as uncertain significance by Gharavi Laboratory,Columbia University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_000053.4(ATP7B):c.2989G>A (p.Val997Met) rs1566485134
NM_000053.4(ATP7B):c.3280_3281insGTAT (p.Phe1094fs) rs1566469148
NM_000053.4(ATP7B):c.3571A>G (p.Met1191Val) rs1566452960
NM_000053.4(ATP7B):c.3680C>A (p.Ala1227Asp) rs1566451314
NM_000053.4(ATP7B):c.4090G>C (p.Val1364Leu) rs1566434432
NM_000053.4(ATP7B):c.811T>C (p.Cys271Arg) rs1349622044

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.