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Sensitive

Ischemic stroke in dyslipidemia

ULK4 · rs3897976

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 295 Korean ancestry cases, 20,474 Korean ancestry controls.

The effect Each copy of the A allele carried 2.16 times the odds of Ischemic stroke in dyslipidemia (95% confidence interval 1.646-2.84); p = 3 × 10−8.

How common The A allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 3, band 3p22.1 — in an intron of ULK4.

How common each version is

AG
Korean KRGDB
A 4.5% · G 95.5%
Korean Korea4K
A 5.2% · G 94.8%
Japanese ToMMo
A 4.4% · G 95.6%
Vietnamese
A 5.2% · G 94.8%
World gnomAD
A 9.2% · G 90.8%
World 1000 Genomes
A 7.5% · G 92.5%
World TOPMed
A 8.8% · G 91.2%

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 Ischemic stroke in dyslipidemia. 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 Ischemic stroke in dyslipidemia. That is a smaller link than two copies.
G/G No copy of the version the research linked to Ischemic stroke in dyslipidemia. This is the starting point the study compared everyone against.
Source

Quoting this page

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Ischemic stroke in dyslipidemia (rs3897976). MyGeneLog™. https://www.mygenelog.com/variants/rs3897976

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