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Standard

Phospholipids to Total Lipids in Very Large HDL percentage

TRIT1 · rs566328102

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−15, with 4 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 434,646 British ancestry individuals, 8,796 British Central/South Asian individuals, 6,573 British African individuals.

The effect Each copy of the T allele shifted the measure 0.02 % higher (95% confidence interval 0.02-0.02); p = 7 × 10−12.

Where it sits Chromosome 1, band 1p34.2 — in an intron of TRIT1.

How common each version is

AT
World 1000 Genomes
A 89.9% · T 10.1%

By ancestry gnomAD

East Asian
A 99.6%
European (non-Finnish)
A 86.2% · T 13.8%
African / African American
A 88.4% · T 11.6%
South Asian
A 83.7% · T 16.3%
Admixed American (Latino)
A 92.9% · T 7.1%

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. The ancestry rows are gnomAD's own groups (via Ensembl), as the survey defines them, not races. No Korean figure for this position yet.

What each result means

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

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Phospholipids to Total Lipids in Very Large HDL percentage (rs566328102). MyGeneLog™. https://www.mygenelog.com/variants/rs566328102

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