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Standard

Lymphoid leukemia, chronic (PheCode 204.12)

ACOXL · rs10202539

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−20, with 2 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 360 African American or Afro-Caribbean cases, 121,531 African American or Afro-Caribbean controls, 2,845 European ancestry cases, 448,087 European ancestry controls.

The effect Each copy of the G allele shifted the measure 0.257 lower (95% confidence interval 0.22-0.3); p = 4 × 10−21.

How common The G allele had a frequency of about 70% in the people studied.

Where it sits Chromosome 2, band 2q13 — in an intron of ACOXL.

How common each version is

AG
Korean KRGDB
A 22.3% · G 77.7%
Korean Korea4K
A 21.9% · G 78.1%
Japanese ToMMo
A 24.3% · G 75.7%
World gnomAD
A 27.4% · G 72.6%
World 1000 Genomes
A 22.9% · G 77.1%
World TOPMed
A 26.3% · G 73.7%

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 Lymphoid leukemia, chronic (PheCode 204.12). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Lymphoid leukemia, chronic (PheCode 204.12). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Lymphoid leukemia, chronic (PheCode 204.12). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Lymphoid leukemia, chronic (PheCode 204.12) (rs10202539). MyGeneLog™. https://www.mygenelog.com/variants/rs10202539

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