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Its strongest genetic-study result is p = 10−28, with 1 associations in the GWAS Catalog.
How this is scored
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 684,122 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.04 lower; p = 1 × 10−28.
Where it sits Chromosome 11, band 11p15.4 — in an intron of SBF2.
What each result means
A/ANo copy of the version the research linked to Hemoglobin levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Hemoglobin levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Hemoglobin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2020 · PMID 32327693 · open access
Questions about rs72855633
What is rs72855633?
rs72855633 is a single position in the genome, in or near the SBF2 gene. Published research associates it with hemoglobin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs72855633 linked to?
On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs72855633 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 rs72855633 come from?
GWAS Catalog, Communications biology 2020, PMID:32327693. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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