Traits - Iron Levels

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Iron Levels

Mineral Absorption

Iron is essential for hemoglobin in red blood cells and for many enzymes. Researchers track several iron biomarkers, including transferrin, ferritin, and serum iron.

Variants in HFE and TMPRSS6, among others, have been linked to differences in iron absorption, transport, and storage.

This result reflects research-level variation in iron-related biology and is not a blood test or a recommendation for iron supplementation.

Dietary iron intake, blood loss (including menstruation), pregnancy, inflammation, GI health, and medications also strongly influence real iron status.

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9 SNP entries
Genes
0
Research
1 study
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Genetic tendency

Average genetic tendency

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Behind this report

Review the genes, tested markers and supporting research.

SNPs tested

These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.

Genotypes and reported variant frequencies
SNPChromosomeGenotypeVariant alleleFrequency
rs4921915AAA78.20%
rs6486121CTT63.10%
rs744653TTT85.40%
rs855791AG44.60%
rs9990333CTT46.00%
rs174577--A33.00%
rs1800562--A6.70%
rs8177179--A52.10%
rs8177240--66.90%

DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.

Research studies

The following peer-reviewed scientific studies support the genetic associations analyzed in this report.

10/29/2014 Nat Commun

Authors: Benyamin B, Esko T, Ried JS, Radhakrishnan A, Vermeulen SH, Traglia M, Gögele M, Anderson D, Broer L, Podmore C, Luan J, Kutalik Z, Sanna S, van der Meer P, Tanaka T, Wang F, Westra HJ, Franke L, Mihailov E, Milani L, Hälldin J, Winkelmann J, Meitinger T, Thiery J, Peters A, Waldenberger M, Rendon A, Jolley J, Sambrook J, Kiemeney LA, Sweep FC, Sala CF, Schwienbacher C, Pichler I, Hui J, Demirkan A, Isaacs A, Amin N, Steri M, Waeber G, Verweij N, Powell JE, Nyholt DR, Heath AC, Madden PA, Visscher PM, Wright MJ, Montgomery GW, Martin NG, Hernandez D, Bandinelli S, van der Harst P, Uda M, Vollenweider P, Scott RA, Langenberg C, Wareham NJ, , van Duijn C, Beilby J, Pramstaller PP, Hicks AA, Ouwehand WH, Oexle K, Gieger C, Metspalu A, Camaschella C, Toniolo D, Swinkels DW, Whitfield JB

Study sample: 23,986 individuals (european ancestry)

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Coverage: 5/9 SNP entries detected (55%).

Reference: Human Genome Build 37 (HG19). Other testing companies may report using the opposite strand, requiring conversion for comparison.

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