rs3811647
rs3811647 is a common intronic marker in TF at GRCh38 3:133765185. In the reviewed G/A model, each A copy is repeatedly linked to more serum transferrin and greater total iron-binding capacity across European, East Asian, and African-ancestry cohorts. Serum iron is null or A-higher in major exact-marker studies, so lower transferrin saturation must not be relabeled as lower general iron. This marker does not measure stored iron, diagnose iron deficiency, or guide supplements. The unstudied C allele is outside the reviewed map.
Traits rs3811647 reads
Gene
Reference databases
How Biome reads this
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