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Standard

Educational attainment (years of education)

ARB2A · rs12332731

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−13, 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 up to 1,131,881 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0135 higher (95% confidence interval 0.01-0.017); p = 6 × 10−14.

How common The A allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 5, band 5q15 — in an intron of ARB2A.

How common each version is

AT
Korean KRGDB
A 5.5% · T 94.5%
Korean Korea4K
A 6.0% · T 94.0%
Japanese ToMMo
A 5.6% · T 94.4%
Vietnamese
A 5.1% · T 94.9%
World gnomAD
A 17.8% · T 82.2%
World 1000 Genomes
A 14.4% · T 85.6%
World TOPMed
A 18.9% · T 81.1%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.

What each result means

A/A Two copies of the version the research linked to Educational attainment (years of education). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Educational attainment (years of education). That is a smaller link than two copies.
T/T No copy of the version the research linked to Educational attainment (years of education). This is the starting point the study compared everyone against.
Source

Quoting this page

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Educational attainment (years of education) (rs12332731). MyGeneLog™. https://www.mygenelog.com/variants/rs12332731

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