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Standard

eosinophil (absolute count, mean, inv-norm transformed)

DYRK1A · rs73218410

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−20, with 6 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 310,757 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.046 higher (95% confidence interval 0.036-0.056); p = 5 × 10−21.

How common The C allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 21, band 21q22.13 — in an intron of DYRK1A.

How common each version is

CT
Japanese ToMMo
C 100.0%
World gnomAD
C 92.5% · T 7.5%
World 1000 Genomes
C 96.8% · T 3.2%
World TOPMed
C 93.3% · T 6.7%

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. No Korean figure for this position yet.

What each result means

C/C Two copies of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Source

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eosinophil (absolute count, mean, inv-norm transformed) (rs73218410). MyGeneLog™. https://www.mygenelog.com/variants/rs73218410

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