SNP information rs9366637
Normal allele: CC
The gene polymorphism is associated with altered blood ferritin levels and increased susceptibility to coronary heart disease.
Polymorphism rs9366637 is related to topics like this:
Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...
Research and publications:
23792061 Meta-analyses of HFE variants in coronary heart disease.
24391736 The contribution of diet and genotype to iron status in women: a classical twin study.
25955080 Birth Characteristics and Childhood Leukemia Risk: Correlations With Genetic Markers.
26054392 Natural selection on HFE in Asian populations contributes to enhanced non-heme iron absorption.
We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...
Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...
Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...