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Standard

Cholesterol levels in chylomicrons and extremely large VLDL

near FIZ1 · rs12610709

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−18, with 47 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 A allele shifted the measure 0.02 mmol/L higher (95% confidence interval 0.02-0.02); p = 3 × 10−14.

Where it sits Chromosome 19, band 19q13.42 — between genes, 0.4 kb from FIZ1.

How common each version is

AG
Korean KRGDB
A 10.4% · G 89.6%
Korean Korea4K
A 11.8% · G 88.2%
Japanese ToMMo
A 12.4% · G 87.6%
Vietnamese
A 27.1% · G 72.9%
World gnomAD
A 14.9% · G 85.1%
World 1000 Genomes
A 15.3% · G 84.7%
World TOPMed
A 15.1% · G 84.9%

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 Cholesterol levels in chylomicrons and extremely large VLDL. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Cholesterol levels in chylomicrons and extremely large VLDL. That is a smaller link than two copies.
G/G No copy of the version the research linked to Cholesterol levels in chylomicrons and extremely large VLDL. This is the starting point the study compared everyone against.
Source

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Cholesterol levels in chylomicrons and extremely large VLDL (rs12610709). MyGeneLog™. https://www.mygenelog.com/variants/rs12610709

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