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Sensitive

Metabolic syndrome

near LPL · rs1837842

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−32, 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 24,171 Taiwanese ancestry cases, 83,059 Taiwanese ancestry controls.

The effect Each copy of the T allele shifted the measure 0.161 lower (95% confidence interval 0.13-0.19); p = 1 × 10−32.

How common The T allele had a frequency of about 18% in the people studied.

Where it sits Chromosome 8, band 8p21.3 — between genes, 43.5 kb from LPL.

How common each version is

CT
Korean KRGDB
C 20.4% · T 79.6%
Korean Korea4K
C 19.9% · T 80.1%
Korean Korea1K
C 20.1% · T 79.9%
Japanese ToMMo
C 19.2% · T 80.8%
Vietnamese
C 18.3% · T 81.7%
World gnomAD
C 22.6% · T 77.4%
World 1000 Genomes
C 20.7% · T 79.3%
World TOPMed
C 22.2% · T 77.8%

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 Metabolic syndrome. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Metabolic syndrome. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Metabolic syndrome. 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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Metabolic syndrome (rs1837842). MyGeneLog™. https://www.mygenelog.com/variants/rs1837842

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