Standard

White blood cell count (neutrophil)

FCRL5 · rs2873345

What the study found

Who was studied 16,201 African American or Afro-Caribbean individuals.

The effect Each copy of the T allele shifted the measure 0.174 lower (95% confidence interval 0.14-0.21); p = 5 × 10−27.

How common The T allele had a frequency of about 41% in the people studied.

Where it sits Chromosome 1, band 1q23.1 — in an intron of FCRL5.

What each result means

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

Questions about rs2873345

What is rs2873345?

rs2873345 is a single position in the genome, in or near the FCRL5 gene. Published research associates it with white blood cell count (neutrophil). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2873345 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 rs2873345 come from?

GWAS Catalog, BMC genomics 2021, PMID:34107879. 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.

White blood cell count (neutrophil) (rs2873345). MyGeneLog™. https://www.mygenelog.com/variants/rs2873345

← See all variants