ClinVar Miner

List of variants in gene DNAH8 reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_001206927.2(DNAH8):c.10963-1G>A rs376903331
NM_001206927.2(DNAH8):c.11563+1G>T rs776791493
NM_001206927.2(DNAH8):c.12007+1G>T rs372080325
NM_001206927.2(DNAH8):c.1516-2A>C rs200115379
NM_001206927.2(DNAH8):c.2139+1G>A rs376576474
NM_001206927.2(DNAH8):c.2664+2T>C
NM_001206927.2(DNAH8):c.3333+1G>A rs756616538
NM_001206927.2(DNAH8):c.6131+1G>A rs145974361
NM_001206927.2(DNAH8):c.763-1G>A rs1582865345
NM_001206927.2(DNAH8):c.9194+1G>A rs144711161
NM_001206927.2(DNAH8):c.9349-1G>T rs1554132747

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.