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Hemoglobin levels

CDK10 · rs447735

Where this position leads

Condition: Blood Cell Counts

rs447735 Condition: Blood Cell Counts Blood Cell Counts Condition rs447735 rs447735 CDK10

What the study found

Who was studied 684,122 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.021 higher; p = 3 × 10−22.

Where it sits Chromosome 16, band 16q24.3 — in an intron of SPATA33.

What each result means

C/C Two 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.
C/T One copy of the version the research linked to Hemoglobin levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Hemoglobin levels. This is the starting point the study compared everyone against.
Source

Questions about rs447735

What is rs447735?

rs447735 is a single position in the genome, in or near the CDK10 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 rs447735 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 rs447735 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 rs447735 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.

Quoting this page

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Hemoglobin levels (rs447735). MyGeneLog™. https://www.mygenelog.com/variants/rs447735

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