Standard

C-C motif chemokine 4 levels

near RN7SL301P · rs2376468

What the study found

Who was studied 21,758 European ancestry individuals; replicated in 9,173 individuals.

The effect Each copy of the C allele shifted the measure 0.134 lower; p = 2 × 10−17.

How common The C allele had a frequency of about 77% in the people studied.

Where it sits Chromosome 17, band 17q12 — between genes, 24.1 kb from RN7SL301P.

What each result means

C/C Two copies of the version the research linked to C-C motif chemokine 4 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to C-C motif chemokine 4 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to C-C motif chemokine 4 levels. This is the starting point the study compared everyone against.
Source

Questions about rs2376468

What is rs2376468?

rs2376468 is a single position in the genome, in or near the near RN7SL301P gene. Published research associates it with c-c motif chemokine 4 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2376468 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 rs2376468 come from?

GWAS Catalog, Nature metabolism 2020, PMID:33067605. 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.

C-C motif chemokine 4 levels (rs2376468). MyGeneLog™. https://www.mygenelog.com/variants/rs2376468

← See all variants