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Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3)

RPS9 · rs73053487

What the study found

Who was studied 3,301 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.62 higher (95% confidence interval 0.46-0.78); p = 1 × 10−13.

How common The C allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 19, band 19q13.42 — inside RPS9.

What each result means

C/C Two copies of the version the research linked to Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3). That is a smaller link than two copies.
T/T No copy of the version the research linked to Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3). This is the starting point the study compared everyone against.
Source

Questions about rs73053487

What is rs73053487?

rs73053487 is a single position in the genome, in or near the RPS9 gene. Published research associates it with leukocyte immunoglobulin-like receptor subfamily a member 6 levels (lilra6.7059.14.3). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs73053487 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 rs73053487 come from?

GWAS Catalog, Nature 2018, PMID:29875488. 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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Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3) (rs73053487). MyGeneLog™. https://www.mygenelog.com/variants/rs73053487

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