Sensitive

Childhood steroid-sensitive nephrotic syndrome

HLA-DRB1 · rs28366266

Where this position leads

Condition: Childhood Steroid-Sensitive Nephrotic Syndrome

rs28366266 Condition: Childhood Steroid-Sensitive Nephrotic Syndrome Childhood Steroid-Sensitive Nephrot… Condition rs28366266 rs28366266 HLA-DRB1

What the study found

Who was studied 244 European ancestry cases, 2,552 European ancestry controls, 56 African cases, 454 African controls, 85 Maghrebian cases, 261 Maghrebian controls.

The effect Each copy of the C allele carried 3.03 times the odds of Childhood steroid-sensitive nephrotic syndrome (95% confidence interval 2.40-3.85); p = 4 × 10−20.

How common The C allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 2.1 kb from HLA-DRB1.

What each result means

C/C Two copies of the version the research linked to Childhood steroid-sensitive nephrotic syndrome. 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 Childhood steroid-sensitive nephrotic syndrome. That is a smaller link than two copies.
T/T No copy of the version the research linked to Childhood steroid-sensitive nephrotic syndrome. This is the starting point the study compared everyone against.
Source

Questions about rs28366266

What is rs28366266?

rs28366266 is a single position in the genome, in or near the HLA-DRB1 gene. Published research associates it with childhood steroid-sensitive nephrotic syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs28366266 linked to?

On MyGeneLog this position is linked to Childhood Steroid-Sensitive Nephrotic Syndrome. The research behind each link, and its sources, are set out on that condition page.

Does having rs28366266 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 rs28366266 come from?

GWAS Catalog, J Am Soc Nephrol 2018, PMID:29903748. 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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Childhood steroid-sensitive nephrotic syndrome (rs28366266). MyGeneLog™. https://www.mygenelog.com/variants/rs28366266

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