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Plateletcrit

RP11-181G12.4 · rs78265569

Where this position leads

Condition: Blood Cell Counts

rs78265569 Condition: Blood Cell Counts Blood Cell Counts Condition rs78265569 rs78265569 RP11-181G12.4

What the study found

Who was studied 164,339 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0404 lower (95% confidence interval 0.028-0.053); p = 5 × 10−10.

How common The A allele had a frequency of about 9% in the people studied.

Where it sits Chromosome 1, band 1p36.33 — in an intron of LOC124903823.

What each result means

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

Questions about rs78265569

What is rs78265569?

rs78265569 is a single position in the genome, in or near the RP11-181G12.4 gene. Published research associates it with plateletcrit. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs78265569 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 rs78265569 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 rs78265569 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Plateletcrit (rs78265569). MyGeneLog™. https://www.mygenelog.com/variants/rs78265569

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