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Standard

Phosphoglycerides levels

ABCB11 · rs3770586

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−9, with 20 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 T allele shifted the measure 0.00317 lower (95% confidence interval 0.0021-0.0042); p = 2 × 10−9.

How common The T allele had a frequency of about 48% in the people studied.

Where it sits Chromosome 2, band 2q31.1 — in an intron of ABCB11.

How common each version is

CT
Korean KRGDB
C 59.0% · T 41.0%
Korean Korea4K
C 59.3% · T 40.7%
Korean Korea1K
C 58.7% · T 41.3%
Japanese ToMMo
C 53.4% · T 46.6%
Vietnamese
C 50.5% · T 49.5%
World gnomAD
C 55.8% · T 44.2%
World 1000 Genomes
C 56.3% · T 43.7%
World TOPMed
C 56.4% · T 43.6%

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 Phosphoglycerides levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Phosphoglycerides levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Phosphoglycerides levels. 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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Phosphoglycerides levels (rs3770586). MyGeneLog™. https://www.mygenelog.com/variants/rs3770586

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