ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
NM_001277115.2(DNAH11):c.10009A>C (p.Ile3337Leu) rs145645790
NM_001277115.2(DNAH11):c.10441G>A (p.Glu3481Lys) rs727502969
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895
NM_001277115.2(DNAH11):c.11186A>T (p.Tyr3729Phe) rs727502970
NM_001277115.2(DNAH11):c.11267G>A (p.Arg3756His) rs554657293
NM_001277115.2(DNAH11):c.12969G>C (p.Gln4323His) rs191802172
NM_001277115.2(DNAH11):c.3494A>G (p.Asp1165Gly) rs370436662
NM_001277115.2(DNAH11):c.3853-12T>A rs727502966
NM_001277115.2(DNAH11):c.470G>A (p.Gly157Glu) rs185011953
NM_001277115.2(DNAH11):c.4879C>T (p.Arg1627Cys) rs727502967
NM_001277115.2(DNAH11):c.4984G>C (p.Asp1662His) rs778565448
NM_001277115.2(DNAH11):c.5537T>A (p.Val1846Asp) rs727502968
NM_001277115.2(DNAH11):c.6152C>T (p.Thr2051Met) rs375341444
NM_001277115.2(DNAH11):c.68C>T (p.Ser23Leu) rs745842220

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.