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Standard

Smoking initiation

near CTNNA2 · rs12993205

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−17, 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 3,382,012 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.00664 higher (95% confidence interval 0.0051-0.0082); p = 3 × 10−17.

How common The T allele had a frequency of about 44% in the people studied.

Where it sits Chromosome 2, band 2p12 — between genes, 144.6 kb from CTNNA2.

How common each version is

CT
Korean KRGDB
C 80.3% · T 19.7%
Korean Korea4K
C 80.6% · T 19.4%
Korean Korea1K
C 81.1% · T 18.9%
Japanese ToMMo
C 78.7% · T 21.3%
Vietnamese
C 72.4% · T 27.6%
World gnomAD
C 64.7% · T 35.3%
World 1000 Genomes
C 71.5% · T 28.5%
World TOPMed
C 65.3% · T 34.6%

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

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

Quoting this page

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Smoking initiation (rs12993205). MyGeneLog™. https://www.mygenelog.com/variants/rs12993205

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