ClinVar Miner

List of variants in gene NEBL reported by Stanford Center for Inherited Cardiovascular Disease, Stanford University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_213569.2(NEBL):c.357+64639A>G rs368268112
NM_213569.2(NEBL):c.357+71749G>C rs41277374
NM_213569.2(NEBL):c.357+71774A>G rs780384504
NM_213569.2(NEBL):c.358-1085C>G rs876661379
NM_213569.2(NEBL):c.358-37463C>A rs146198369
NM_213569.2(NEBL):c.358-45331A>G rs147853594

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.