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Standard

Pneumonia due to fungus (mycoses) (PheCode 480.3)

TG · rs377366255

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−11, 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 424 African American or Afro-Caribbean cases, 120,597 African American or Afro-Caribbean controls, 1,297 European ancestry cases, 446,537 European ancestry controls.

The effect Each copy of the C allele shifted the measure 2.9 lower (95% confidence interval 2.87-2.93); p = 1 × 10−11.

How common The C allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 8, band 8q24.22 — in an intron of TG.

How common each version is

AC
World gnomAD
A 0.0% · C 100.0%
World 1000 Genomes
A 0.0% · C 100.0%
World TOPMed
A 0.0% · C 100.0%

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

A/A No copy of the version the research linked to Pneumonia due to fungus (mycoses) (PheCode 480.3). This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Pneumonia due to fungus (mycoses) (PheCode 480.3). That is a smaller link than two copies.
C/C Two copies of the version the research linked to Pneumonia due to fungus (mycoses) (PheCode 480.3). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Pneumonia due to fungus (mycoses) (PheCode 480.3) (rs377366255). MyGeneLog™. https://www.mygenelog.com/variants/rs377366255

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