ClinVar Miner

List of variants in gene ZNF41 reported as benign for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
NM_007130.3(ZNF41):c.*407A>G rs3810664
NM_007130.3(ZNF41):c.-231A>G rs5905607
NM_007130.3(ZNF41):c.374T>G (p.Ile125Arg) rs17147624
NM_007130.3(ZNF41):c.387A>G (p.Ser129=) rs60022654
NM_007130.3(ZNF41):c.65C>T (p.Ser22Leu) rs184685998
NM_007130.3(ZNF41):c.660T>G (p.Asn220Lys) rs34301930
NM_007130.3(ZNF41):c.901T>C (p.Cys301Arg) rs34391244

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.