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Standard

Monocyte count

IK · rs56692296

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, with 1 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 408,112 British individuals.

The effect Each copy of the A allele shifted the measure 0.0174 higher (95% confidence interval 0.012-0.023); p = 1 × 10−10.

How common The A allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 5, band 5q31.3 — in an intron of IK.

How common each version is

AG
Korean KRGDB
A 27.0% · G 73.0%
Korean Korea4K
A 25.3% · G 74.7%
Korean Korea1K
A 28.1% · G 71.9%
Japanese ToMMo
A 29.9% · G 70.1%
Vietnamese
A 29.3% · G 70.7%
World gnomAD
A 17.2% · G 82.8%
World 1000 Genomes
A 18.1% · G 81.9%
World TOPMed
A 15.9% · G 84.1%

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 Monocyte count. 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 Monocyte count. That is a smaller link than two copies.
G/G No copy of the version the research linked to Monocyte count. This is the starting point the study compared everyone against.
Source

Quoting this page

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Monocyte count (rs56692296). MyGeneLog™. https://www.mygenelog.com/variants/rs56692296

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