ClinVar Miner

List of variants in gene combination COL6A2, FTCD reported as benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_001849.3(COL6A2):c.*158C>T rs11554666
NM_001849.3(COL6A2):c.2724A>G (p.Thr908=) rs9977394
NM_206965.2(FTCD):c.1470C>T (p.Gly490=) rs10432965

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.