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Standard

Monocyte count

NFKB1-AS1 · rs141936164

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−21, with 3 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 521,594 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0187 SD unit lower (95% confidence interval 0.015-0.023); p = 2 × 10−21.

How common The G allele had a frequency of about 35% in the people studied.

Where it sits Chromosome 4, band 4q24 — in an intron of NFKB1-AS1.

How common each version is

AG
Korean KRGDB
A 64.6% · G 35.4%
Korean Korea4K
A 66.5% · G 33.5%
Korean Korea1K
A 66.1% · G 33.9%
Japanese ToMMo
A 68.0% · G 31.9%
Vietnamese
A 61.3% · G 38.7%
World gnomAD
A 72.9% · G 27.1%
World 1000 Genomes
A 75.5% · G 24.5%
World TOPMed
A 73.2% · G 26.9%

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 (rs141936164). MyGeneLog™. https://www.mygenelog.com/variants/rs141936164

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