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Standard

Apolipoprotein A1 levels

CHD9 · rs12598179

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 393,193 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0124 lower (95% confidence interval 0.0081-0.0166); p = 1 × 10−8.

How common The G allele had a frequency of about 71% in the people studied.

Where it sits Chromosome 16, band 16q12.2 — between genes, 3.7 kb from RNA5SP427.

How common each version is

CG
Korean KRGDB
C 17.9% · G 82.1%
Korean Korea4K
C 19.1% · G 80.9%
Korean Korea1K
C 18.5% · G 81.5%
Japanese ToMMo
C 17.0% · G 83.0%
Vietnamese
C 25.7% · G 74.3%
World gnomAD
C 28.1% · G 71.9%
World 1000 Genomes
C 26.9% · G 73.1%
World TOPMed
C 27.9% · G 72.1%

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

C/C No copy of the version the research linked to Apolipoprotein A1 levels. This is the starting point the study compared everyone against.
C/G One copy of the version the research linked to Apolipoprotein A1 levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Apolipoprotein A1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Apolipoprotein A1 levels (rs12598179). MyGeneLog™. https://www.mygenelog.com/variants/rs12598179

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