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Intelligence

DCC · rs62100775

Where this position leads

Condition: Intelligence

rs62100775 Condition: Intelligence Intelligence Condition rs62100775 rs62100775 DCC

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 5.71 z-score higher; p = 1 × 10−8.

Where it sits Chromosome 18, band 18q21.2 — in an intron of DCC.

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 rs62100775

What is rs62100775?

rs62100775 is a single position in the genome, in or near the DCC 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 rs62100775 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 rs62100775 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 rs62100775 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

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.

Intelligence (rs62100775). MyGeneLog™. https://www.mygenelog.com/variants/rs62100775

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