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Hemoglobin concentration

NOTCH4 · rs3132956

What the study found

Who was studied 46,904 European ancestry males; replicated in 80,822 European ancestry males.

The effect Each copy of the A allele shifted the measure 0.0483 lower; p = 2 × 10−20.

How common The A allele had a frequency of about 15% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — in an intron of NOTCH4.

What each result means

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

Questions about rs3132956

What is rs3132956?

rs3132956 is a single position in the genome, in or near the NOTCH4 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 rs3132956 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 rs3132956 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 (rs3132956). MyGeneLog™. https://www.mygenelog.com/variants/rs3132956

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