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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 116,666 British ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0259 higher (95% confidence interval 0.018-0.034); p = 2 × 10−10.
Where it sits Chromosome 5, band 5q35.2 — between genes, 32.4 kb from CEP192P1.
What each result means
G/GNo copy of the version the research linked to Red cell distribution width. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Red cell distribution width. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Red cell distribution width. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs7735282 is a single position in the genome, in or near the LOC643201 gene. Published research associates it with red cell distribution width. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7735282 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 rs7735282 come from?
GWAS Catalog, PloS one 2017, PMID:28957414. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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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.
Red cell distribution width (rs7735282). MyGeneLog™. https://www.mygenelog.com/variants/rs7735282