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Neutrophil side scatter

ARSB · rs4704532

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10⁻⁶², 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 38,341 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.155 SD units lower (95% confidence interval 0.14-0.17); p = 1 × 10⁻⁶².

How common The T allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 5, band 5q14.1 — in an intron of ARSB.

How common each version is

CT

Korean KRGDB

C 99.4% · T 0.6%

Korean Korea4K

C 99.6% · T 0.4%

Korean Korea1K

C 99.8% · T 0.2%

Japanese ToMMo

C 99.7% · T 0.3%

Vietnamese

C 99.5% · T 0.5%

World gnomAD

C 86.4% · T 13.6%

World 1000 Genomes

C 89.0% · T 11.0%

World TOPMed

C 86.1% · T 13.9%

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

C/C No copy of the version the research linked to Neutrophil side scatter. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to Neutrophil side scatter. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Neutrophil side scatter. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology

Akbari P, Vuckovic D, Stefanucci L, Jiang T, Kundu K, Kreuzhuber R, Bao EL, Collins JH, Downes K, Grassi L, Guerrero JA, Kaptoge S

and 20 more — show all

Nature communications · 2023 · PMID 37596262 · open access

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Neutrophil side scatter (rs4704532). MyGeneLog™. https://www.mygenelog.com/variants/rs4704532

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