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Standard

Linoleic acid to total fatty acids percentage

near PLG · rs6935921

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−24, 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 = 3 × 10−24.

Where it sits Chromosome 6, band 6q26 — between genes, 14.6 kb from PLG.

How common each version is

CT
Korean KRGDB
C 57.6% · T 42.4%
Korean Korea4K
C 58.1% · T 41.9%
Korean Korea1K
C 56.9% · T 43.1%
Japanese ToMMo
C 61.2% · T 38.8%
Vietnamese
C 72.6% · T 27.4%
World gnomAD
C 36.1% · T 63.9%
World 1000 Genomes
C 46.5% · T 53.5%
World TOPMed
C 37.5% · T 62.5%

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

C/C No copy of the version the research linked to Linoleic acid to total fatty acids percentage. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Linoleic acid to total fatty acids percentage. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Linoleic acid to total fatty acids percentage. 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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Linoleic acid to total fatty acids percentage (rs6935921). MyGeneLog™. https://www.mygenelog.com/variants/rs6935921

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