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SNP information rs1880669

RS1880669

Normal allele: CC

Single nucleotide polymorphisms in genes associated with serum iron and ferritin levels.

Polymorphism rs1880669 is related to topics like this:

Genetic haemochromatosis

Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...

Research and publications:

  19673882   A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.

  20215856   Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head.

  22761678   Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.

  24121126   Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.

  28917245   A single-nucleotide polymorphism in transferrin is associated with soluble transferrin receptor in Chinese adolescents.

  29936663   Associations of TF Gene Polymorphisms with the Risk of Ischemic Stroke.

DNA test for autism

We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...

Gene for lactose intolerance

Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...

CCNB1 cyclin B1

Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...

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