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Red cell distribution width

LINC01149 · rs2523696

What the study found

Who was studied 171,529 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0276 higher (95% confidence interval 0.021-0.035); p = 9 × 10−15.

How common The T allele had a frequency of about 44% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — in a non-coding transcript of LINC01149.

What each result means

C/C No copy of the version the research linked to Red cell distribution width. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Red cell distribution width. That is a smaller link than two copies.
T/T Two 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.
Source

Questions about rs2523696

What is rs2523696?

rs2523696 is a single position in the genome, in or near the LINC01149 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 rs2523696 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 rs2523696 come from?

GWAS Catalog, Cell 2016, PMID:27863252. 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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Red cell distribution width (rs2523696). MyGeneLog™. https://www.mygenelog.com/variants/rs2523696

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