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CD33 on CD33+ HLA DR+ CD14-

CD33 · rs116623489

What the study found

Who was studied 1,578 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the T allele shifted the measure 1.08 lower (95% confidence interval 0.73-1.42); p = 1 × 10−9.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 19, band 19q13.41 — in an intron of CD33.

What each result means

C/C No copy of the version the research linked to CD33 on CD33+ HLA DR+ CD14-. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to CD33 on CD33+ HLA DR+ CD14-. That is a smaller link than two copies.
T/T Two copies of the version the research linked to CD33 on CD33+ HLA DR+ CD14-. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs116623489

What is rs116623489?

rs116623489 is a single position in the genome, in or near the CD33 gene. Published research associates it with cd33 on cd33+ hla dr+ cd14-. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs116623489 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 rs116623489 come from?

GWAS Catalog, Nature genetics 2020, PMID:32929287. 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.

CD33 on CD33+ HLA DR+ CD14- (rs116623489). MyGeneLog™. https://www.mygenelog.com/variants/rs116623489

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