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Sensitive

Lung adenocarcinoma

GAREM1 · rs638868

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−7, 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 11,753 East Asian ancestry cases, 30,562 East Asian ancestry controls, 11,273 European ancestry cases, 55,483 European ancestry controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 4 × 10−8.

Where it sits Chromosome 18, band 18q12.1 — in an intron of GAREM1.

How common each version is

AC
Korean KRGDB
A 79.9% · C 20.1%
Korean Korea4K
A 80.5% · C 19.5%
Korean Korea1K
A 81.3% · C 18.7%
Japanese ToMMo
A 76.3% · C 23.7%
Vietnamese
A 74.8% · C 25.2%
World gnomAD
A 67.4% · C 32.6%
World 1000 Genomes
A 67.4% · C 32.6%
World TOPMed
A 67.2% · C 32.8%

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 No copy of the version the research linked to Lung adenocarcinoma. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Lung adenocarcinoma. That is a smaller link than two copies.
C/C Two copies of the version the research linked to Lung adenocarcinoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Quoting this page

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Lung adenocarcinoma (rs638868). MyGeneLog™. https://www.mygenelog.com/variants/rs638868

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