Upload the DNA data file of the test

23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage

and get an enhanced
personalized health report
free without registration

Files accepted .txt, .csv, .zip, .csv.gz

File data is not stored on the server

SNP information rs7385804

RS7385804

Normal allele: AA

Genetic variation associated with iron overload, chronic anaemia and motor neurone disease.

Polymorphism rs7385804 is related to topics like this:

Genetic haemochromatosis

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


Research and publications:

  19820697   A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

  19862010   Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

  21153663   Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

  21208937   Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

  22323359   TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.

  23751596   Association between genetic variations in TFR2 gene and coronary heart disease in Chinese: a case-control study.

  26159428   Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?

  27332551   Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry.

  31936202   The Prevalence of Insomnia and the Link between Iron Metabolism Genes Polymorphisms, TF rs1049296 C>T, TF rs3811647 G>A, TFR rs7385804 A>C, HAMP rs10421768 A>G and Sleep Disorders in Polish Individuals with ASD.

  32895881   The Proteomics Study of Compounded HFE/TF/TfR2/HJV Genetic Variations in a Thai Family with Iron Overload, Chronic Anemia, and Motor Neuron Disorder.

  35682458   Hepcidin (rs10421768), Transferrin (rs3811647, rs1049296) and Transferrin Receptor 2 (rs7385804) Gene Polymorphism Might Be Associated with the Origin of Multiple Sclerosis.

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...

en
|
de
|
fr
|
es
|
it
|
ua
|
ru

Support