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Standard

Average diameter for VLDL particles

ARNILA · rs11903847

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, with 8 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 C allele shifted the measure 0.01 nm higher (95% confidence interval 0.01-0.01); p = 1 × 10−10.

Where it sits Chromosome 2, band 2p23.3 — in an intron of ARNILA.

How common each version is

CT
Korean KRGDB
C 66.5% · T 33.5%
Korean Korea4K
C 67.2% · T 32.8%
Korean Korea1K
C 66.2% · T 33.8%
Japanese ToMMo
C 63.7% · T 36.3%
Vietnamese
C 61.1% · T 38.9%
World gnomAD
C 63.8% · T 36.2%
World 1000 Genomes
C 61.4% · T 38.6%
World TOPMed
C 61.9% · T 38.1%

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

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

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Average diameter for VLDL particles (rs11903847). MyGeneLog™. https://www.mygenelog.com/variants/rs11903847

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