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Standard

Monocyte count

MEIS1 · rs62144048

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−12, 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 639,696 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals.

The effect The reported allele is G; the catalogue records no effect size ; p = 2 × 10−12.

How common The G allele had a frequency of about 18% in the people studied.

Where it sits Chromosome 2, band 2p14 — in an intron of MEIS1.

How common each version is

AG
Korean Korea4K
A 87.9% · G 12.1%
Japanese ToMMo
A 82.2% · G 17.8%
Vietnamese
A 69.3% · G 30.7%
World gnomAD
A 69.2% · G 30.8%
World 1000 Genomes
A 62.6% · G 37.4%
World TOPMed
A 67.7% · G 32.3%

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 Monocyte count. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Monocyte count. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Monocyte count. 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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Monocyte count (rs62144048). MyGeneLog™. https://www.mygenelog.com/variants/rs62144048

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