ClinVar Miner

List of variants in gene CD46 reported as likely benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_172351.3(CD46):c.-11C>A
NM_172351.3(CD46):c.1103C>T (p.Thr368Ile) rs146803767
NM_172351.3(CD46):c.417A>G (p.Leu139=) rs12126088
NM_172351.3(CD46):c.796G>A (p.Asp266Asn) rs17006830
NM_172351.3(CD46):c.861G>A (p.Ser287=) rs17006843
NM_172351.3(CD46):c.926C>T (p.Pro309Leu)

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.