Sensitive

T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51)

LY9 · rs114914487

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−21, 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 466 African American individuals.

The effect Each copy of the G allele shifted the measure 1.55 higher (95% confidence interval 1.24-1.86); p = 1 × 10−21.

How common The G allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 1, band 1q23.3 — in an intron of LY9.

What each result means

A/A No copy of the version the research linked to T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51). That is a smaller link than two copies.
G/G Two copies of the version the research linked to T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs114914487

What is rs114914487?

rs114914487 is a single position in the genome, in or near the LY9 gene. Published research associates it with t-lymphocyte surface antigen ly-9 level in chronic kidney disease with hypertension and no diabetes (3324_51). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs114914487 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 rs114914487 come from?

GWAS Catalog, Kidney international 2022, PMID:35870639. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51) (rs114914487). MyGeneLog™. https://www.mygenelog.com/variants/rs114914487

← See all variants