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Urea levels

SLC14A2 · rs62093664

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−9, 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 342,286 European ancestry individuals, 6,015 African ancestry individuals, 7,336 South Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0245 higher (95% confidence interval 0.017-0.032); p = 4 × 10−10.

Where it sits Chromosome 18, band 18q12.3 — in an intron of SLC14A2.

What each result means

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

Questions about rs62093664

What is rs62093664?

rs62093664 is a single position in the genome, in or near the SLC14A2 gene. Published research associates it with urea levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs62093664 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs62093664 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Urea levels (rs62093664). MyGeneLog™. https://www.mygenelog.com/variants/rs62093664

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