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Hemoglobin concentration

near OR2W4P · rs13214703

What the study found

Who was studied 52,141 European ancestry females; replicated in 89,584 European ancestry females.

The effect Each copy of the C allele shifted the measure 0.0831 higher; p = 2 × 10−46.

How common The C allele had a frequency of about 9% in the people studied.

Where it sits Chromosome 6, band 6p22.1 — between genes, 3.5 kb from OR2W4P.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hemoglobin concentration compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hemoglobin concentration.
T/T Published research associates this genotype with typical/baseline likelihood of Hemoglobin concentration — no copies of the reported risk allele.
Source

Questions about rs13214703

What is rs13214703?

rs13214703 is a single position in the genome, in or near the near OR2W4P gene. Published research associates it with hemoglobin concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13214703 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs13214703 come from?

GWAS Catalog, The Journal of nutritional biochemistry 2023, PMID:35964923. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Hemoglobin concentration (rs13214703). MyGeneLog™. https://www.mygenelog.com/variants/rs13214703

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