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Standard

Triglyceride levels

LCORL · rs73098804

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−13, 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 153,950 Korean ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0318 higher (95% confidence interval 0.023-0.04); p = 2 × 10−13.

How common The A allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 4, band 4p15.31 — in an intron of LCORL.

How common each version is

AT
Korean KRGDB
A 18.4% · T 81.6%
Korean Korea4K
A 17.8% · T 82.2%
Korean Korea1K
A 17.6% · T 82.4%
Japanese ToMMo
A 19.7% · T 80.3%
Vietnamese
A 28.0% · T 72.0%
World gnomAD
A 14.8% · T 85.2%
World 1000 Genomes
A 20.1% · T 80.0%
World TOPMed
A 15.6% · T 84.5%

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

Quoting this page

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Triglyceride levels (rs73098804). MyGeneLog™. https://www.mygenelog.com/variants/rs73098804

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