red cell diameter width (RDW, mean, inv-norm transformed)
CHADL · rs5751069
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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 110,558 African American or Afro-Caribbean individuals, 51,938 Hispanic or Latin American individuals, 5,549 East Asian ancestry individuals, 380,796 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0239 higher (95% confidence interval 0.018-0.03); p = 3 × 10−16.
How common The C allele had a frequency of about 66% in the people studied.
Where it sits Chromosome 22, band 22q13.2 — in an intron of CHADL.
What each result means
C/CTwo copies of the version the research linked to red cell diameter width (RDW, mean, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to red cell diameter width (RDW, mean, inv-norm transformed). That is a smaller link than two copies.
G/GNo copy of the version the research linked to red cell diameter width (RDW, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs5751069
What is rs5751069?
rs5751069 is a single position in the genome, in or near the CHADL gene. Published research associates it with red cell diameter width (rdw, mean, 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 rs5751069 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 rs5751069 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.
0 10226Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others6Total10Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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