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Standard

Smoking initiation

near TRIOBP · rs11703775

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−26, 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 2,669,029 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0101 lower (95% confidence interval 0.0082-0.012); p = 2 × 10−26.

How common The C allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 22, band 22q13.1 — between genes, 10.8 kb from TRIOBP.

How common each version is

CG
Korean KRGDB
C 35.0% · G 65.0%
Korean Korea4K
C 35.6% · G 64.4%
Korean Korea1K
C 35.3% · G 64.7%
Japanese ToMMo
C 42.9% · G 57.1%
World gnomAD
C 25.4% · G 74.6%
World 1000 Genomes
C 26.6% · G 73.4%
World TOPMed
C 24.4% · G 75.6%

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 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.
C/G One copy of the version the research linked to Smoking initiation. That is a smaller link than two copies.
G/G No copy of the version the research linked to Smoking initiation. This is the starting point the study compared everyone against.
Source

Quoting this page

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Smoking initiation (rs11703775). MyGeneLog™. https://www.mygenelog.com/variants/rs11703775

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