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Standard

Lesions of stomach and duodenum (PheCode 537.1)

SDK1 · rs572678504

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 353 African American or Afro-Caribbean cases, 121,124 African American or Afro-Caribbean controls, 815 European ancestry cases, 449,335 European ancestry controls.

The effect Each copy of the G allele shifted the measure 2.98 lower (95% confidence interval 2.95-3.01); p = 2 × 10−11.

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

Where it sits Chromosome 7, band 7p22.2 — in an intron of SDK1.

How common each version is

AG
World gnomAD
G 100.0%
World 1000 Genomes
A 0.0% · G 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 Lesions of stomach and duodenum (PheCode 537.1). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Lesions of stomach and duodenum (PheCode 537.1). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Lesions of stomach and duodenum (PheCode 537.1). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Lesions of stomach and duodenum (PheCode 537.1) (rs572678504). MyGeneLog™. https://www.mygenelog.com/variants/rs572678504

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