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Standard

Neutrophil-to-lymphocyte ratio

near HLA-DQB1 · rs28532217

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−25, 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 234,502 European ancestry individuals; replicated in 100,442 European ancestry individuals.

The effect The reported allele is C; the catalogue records no effect size ; p = 8 × 10−26.

How common The C allele had a frequency of about 88% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 3.4 kb from HLA-DQB1.

How common each version is

CT
Korean KRGDB
C 79.7% · T 20.3%
Korean Korea4K
C 81.5% · T 18.5%
Japanese ToMMo
C 87.2% · T 12.8%
World gnomAD
C 72.0% · T 28.0%
World 1000 Genomes
C 82.5% · T 17.5%

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

C/C Two copies of the version the research linked to Neutrophil-to-lymphocyte ratio. 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 Neutrophil-to-lymphocyte ratio. That is a smaller link than two copies.
T/T No copy of the version the research linked to Neutrophil-to-lymphocyte ratio. This is the starting point the study compared everyone against.
Source

Quoting this page

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Neutrophil-to-lymphocyte ratio (rs28532217). MyGeneLog™. https://www.mygenelog.com/variants/rs28532217

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