ClinVar Miner

List of variants in gene RUNX1 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
NM_001754.4(RUNX1):c.*44C>G rs535532916
NM_001754.4(RUNX1):c.1044C>T (p.His348=) rs773671764
NM_001754.4(RUNX1):c.1275G>A (p.Pro425=) rs886038488
NM_001754.4(RUNX1):c.167T>C (p.Leu56Ser) rs111527738
NM_001754.4(RUNX1):c.183G>A (p.Pro61=) rs76558016
NM_001754.4(RUNX1):c.729A>C (p.Pro243=) rs999807714
NM_001754.4(RUNX1):c.984A>G (p.Thr328=) rs377305704

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.