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Sensitive

Metabolic syndrome

near LPL · rs1372341

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−27, 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 0.153 lower (95% confidence interval 0.13-0.18); p = 5 × 10−28.

How common The T allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 8, band 8p21.3 — between genes, 46.6 kb from LPL.

How common each version is

AT
Korean KRGDB
A 20.2% · T 79.8%
Korean Korea4K
A 19.6% · T 80.4%
Korean Korea1K
A 19.7% · T 80.3%
Japanese ToMMo
A 18.6% · T 81.4%
World gnomAD
A 36.6% · T 63.4%
World 1000 Genomes
A 29.4% · T 70.6%
World TOPMed
A 35.9% · T 64.1%

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

A/A No copy of the version the research linked to Metabolic syndrome. This is the starting point the study compared everyone against.
A/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 (rs1372341). MyGeneLog™. https://www.mygenelog.com/variants/rs1372341

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