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Standard

Cholesteryl Esters to Total Lipids in Very Small VLDL percentage

PRELID1 · rs4073745

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, with 3 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 G allele shifted the measure 0.01 % higher (95% confidence interval 0.01-0.01); p = 7 × 10−11.

Where it sits Chromosome 5, band 5q35.3 — in the 3′ untranslated region of PRELID1.

How common each version is

AG
Korean KRGDB
A 96.4% · G 3.6%
Korean Korea4K
A 96.6% · G 3.4%
Japanese ToMMo
A 97.5% · G 2.5%
World gnomAD
A 59.4% · G 40.6%
World 1000 Genomes
A 62.6% · G 37.4%
World TOPMed
A 58.3% · G 41.7%

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 Cholesteryl Esters to Total Lipids in Very Small VLDL percentage. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Cholesteryl Esters to Total Lipids in Very Small VLDL percentage. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Cholesteryl Esters to Total Lipids in Very Small VLDL percentage. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Cholesteryl Esters to Total Lipids in Very Small VLDL percentage (rs4073745). MyGeneLog™. https://www.mygenelog.com/variants/rs4073745

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