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Standard

COVID-19 (hospitalized covid vs population)

KCNN3 · rs139589338

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, 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 4,702 Admixed Latin American ancestry cases, 68,573 Admixed Latin American ancestry controls, European, African, East Asian, South Asian or Admixed American individuals (See The COVID-19 Host Genetics Initiative, v7 ALL B2).

The effect Each copy of the A allele shifted the measure 0.191 lower (95% confidence interval 0.13-0.26); p = 1 × 10−8.

Where it sits Chromosome 1, band 1q21.3 — in an intron of KCNN3.

How common each version is

AG
Korean KRGDB
A 100.0% · G 0.0%
Korean Korea1K
A 100.0% · G 0.1%
World gnomAD
A 98.4% · G 1.6%
World 1000 Genomes
A 99.1% · G 0.9%
World TOPMed
A 98.5% · G 1.5%

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

A/A Two copies of the version the research linked to COVID-19 (hospitalized covid vs population). 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 COVID-19 (hospitalized covid vs population). That is a smaller link than two copies.
G/G No copy of the version the research linked to COVID-19 (hospitalized covid vs population). This is the starting point the study compared everyone against.
Source

Quoting this page

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COVID-19 (hospitalized covid vs population) (rs139589338). MyGeneLog™. https://www.mygenelog.com/variants/rs139589338

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