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Normal allele: CC
A polymorphism of the transmembrane serine protease gene is associated with iron deficiency.
Polymorphism rs2111833 is related to topics like this:
Genetic haemochromatosis Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...
Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...
Research and publications:
22761678 Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.
25416640 Inter-ethnic differences in genetic variants within the transmembrane protease, serine 6 (TMPRSS6) gene associated with iron status indicators: a systematic review with meta-analyses.
25741868 Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
25976471 Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.
29928945 The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia.
30593316 [Association between the polymorphisms of TMPRSS6 and the levels of serum ferrtin and soluble transferrin receptor in pregnant women in Lüliang Area of Shanxi Province].
32422234 Study the association of transmembrane serine protease 6 gene polymorphisms with iron deficiency status in Saudi Arabia.
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...