ClinVar Miner

List of variants reported as likely benign for Microcytic anemia

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_001374504.1(TMPRSS6):c.*411C>T
NM_001374504.1(TMPRSS6):c.*72G>T
NM_001374504.1(TMPRSS6):c.1672+9T>C rs200801061
NM_001374504.1(TMPRSS6):c.307C>T (p.Arg103Cys)
NM_001374504.1(TMPRSS6):c.406G>A (p.Glu136Lys)
NM_153609.3(TMPRSS6):c.*576C>A rs139014458
NM_153609.3(TMPRSS6):c.1019C>T (p.Thr340Met) rs185482276
NM_153609.3(TMPRSS6):c.1336C>T (p.Arg446Trp) rs117576908
NM_153609.3(TMPRSS6):c.2383G>A (p.Val795Ile) rs139105452

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.