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Intelligence

near PLCL1 · rs1455344

Where this position leads

Condition: Intelligence

rs1455344 Condition: Intelligence Intelligence Condition rs1455344 rs1455344 near PLCL1

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 269,867 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 5.84 z-score lower; p = 5 × 10−9.

Where it sits Chromosome 2, band 2q33.1 — between genes, 78.8 kb from PLCL1.

What each result means

A/A Two copies of the version the research linked to Intelligence. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Intelligence. That is a smaller link than two copies.
G/G No copy of the version the research linked to Intelligence. This is the starting point the study compared everyone against.
Source

Questions about rs1455344

What is rs1455344?

rs1455344 is a single position in the genome, in or near the near PLCL1 gene. Published research associates it with intelligence. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1455344 linked to?

On MyGeneLog this position is linked to Intelligence. The research behind each link, and its sources, are set out on that condition page.

Does having rs1455344 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 rs1455344 come from?

GWAS Catalog, Nature genetics 2018, PMID:29942086. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Intelligence (rs1455344). MyGeneLog™. https://www.mygenelog.com/variants/rs1455344

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