Standard

platelet count (maximum, inv-norm transformed)

CD109 · rs114709397

What the study found

Who was studied 114,580 African American or Afro-Caribbean individuals.

The effect Each copy of the C allele shifted the measure 0.0643 lower (95% confidence interval 0.051-0.077); p = 1 × 10−22.

How common The C allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 6, band 6q13 — in an intron of CD109.

What each result means

C/C Two copies of the version the research linked to platelet count (maximum, inv-norm transformed). 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 platelet count (maximum, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to platelet count (maximum, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs114709397

What is rs114709397?

rs114709397 is a single position in the genome, in or near the CD109 gene. Published research associates it with platelet count (maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs114709397 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 rs114709397 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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platelet count (maximum, inv-norm transformed) (rs114709397). MyGeneLog™. https://www.mygenelog.com/variants/rs114709397

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