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Standard

Drinks per week

CTNNA2 · rs12992410

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−12, 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 2,965,643 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.00623 lower (95% confidence interval 0.0045-0.0079); p = 7 × 10−13.

How common The A allele had a frequency of about 37% in the people studied.

Where it sits Chromosome 2, band 2p12 — in an intron of CTNNA2.

How common each version is

AG
Korean KRGDB
A 42.4% · G 57.6%
Korean Korea4K
A 43.3% · G 56.7%
Korean Korea1K
A 43.3% · G 56.7%
Japanese ToMMo
A 48.1% · G 51.9%
Vietnamese
A 44.0% · G 56.0%
World gnomAD
A 28.0% · G 72.0%
World 1000 Genomes
A 24.5% · G 75.5%
World TOPMed
A 27.4% · G 72.6%

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 Drinks per week. 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 Drinks per week. That is a smaller link than two copies.
G/G No copy of the version the research linked to Drinks per week. This is the starting point the study compared everyone against.
Source

Quoting this page

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Drinks per week (rs12992410). MyGeneLog™. https://www.mygenelog.com/variants/rs12992410

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