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Lymphocyte count

CFAP97D2 · rs547320937

Where this position leads

Condition: Blood Cell Counts

rs547320937 Condition: Blood Cell Counts Blood Cell Counts Condition rs547320937 rs547320937 CFAP97D2

What the study found

Who was studied 171,643 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.161 lower (95% confidence interval 0.11-0.21); p = 3 × 10−9.

How common The A allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 13, band 13q34 — in an intron of CFAP97D2.

What each result means

A/A Two copies of the version the research linked to Lymphocyte count. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Lymphocyte count. That is a smaller link than two copies.
G/G No copy of the version the research linked to Lymphocyte count. This is the starting point the study compared everyone against.
Source

Questions about rs547320937

What is rs547320937?

rs547320937 is a single position in the genome, in or near the CFAP97D2 gene. Published research associates it with lymphocyte count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs547320937 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 rs547320937 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 rs547320937 come from?

GWAS Catalog, Cell 2016, PMID:27863252. 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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Lymphocyte count (rs547320937). MyGeneLog™. https://www.mygenelog.com/variants/rs547320937

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