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Neutrophil count

TERT · rs6897196

Where this position leads

Condition: Blood Cell Counts

rs6897196 Condition: Blood Cell Counts Blood Cell Counts Condition rs6897196 rs6897196 TERT

What the study found

Who was studied 78,744 East Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0411 SD units lower (95% confidence interval 0.029-0.054); p = 1 × 10−10.

How common The A allele had a frequency of about 64% in the people studied.

Where it sits Chromosome 5, band 5p15.33 — in an intron of TERT.

What each result means

A/A Two copies of the version the research linked to Neutrophil 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 Neutrophil count. That is a smaller link than two copies.
G/G No copy of the version the research linked to Neutrophil count. This is the starting point the study compared everyone against.
Source

Questions about rs6897196

What is rs6897196?

rs6897196 is a single position in the genome, in or near the TERT gene. Published research associates it with neutrophil 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 rs6897196 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 rs6897196 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 rs6897196 come from?

GWAS Catalog, Cell 2020, PMID:32888493. 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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Neutrophil count (rs6897196). MyGeneLog™. https://www.mygenelog.com/variants/rs6897196

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