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Standard

Free cholesterol in small LDL

near PLG · rs6455698

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−9, with 6 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 98,316 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.000797 lower (95% confidence interval 0.00052-0.00107); p = 5 × 10−9.

How common The G allele had a frequency of about 30% in the people studied.

Where it sits Chromosome 6, band 6q26 — between genes, 14.3 kb from PLG.

How common each version is

GT
Korean KRGDB
G 57.6% · T 42.4%
Korean Korea4K
G 58.2% · T 41.8%
Korean Korea1K
G 56.9% · T 43.1%
Japanese ToMMo
G 61.3% · T 38.8%
Vietnamese
G 73.8% · T 26.2%
World gnomAD
G 36.4% · T 63.6%
World 1000 Genomes
G 46.7% · T 53.3%
World TOPMed
G 37.8% · T 62.2%

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

G/G Two copies of the version the research linked to Free cholesterol in small LDL. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/T One copy of the version the research linked to Free cholesterol in small LDL. That is a smaller link than two copies.
T/T No copy of the version the research linked to Free cholesterol in small LDL. This is the starting point the study compared everyone against.
Source

Quoting this page

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Free cholesterol in small LDL (rs6455698). MyGeneLog™. https://www.mygenelog.com/variants/rs6455698

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