Standard

Resistin levels

XAB2 · rs4134826

What the study found

Who was studied 21,758 European ancestry individuals; replicated in 9,173 individuals.

The effect Each copy of the T allele shifted the measure 0.0893 lower; p = 3 × 10−14.

How common The T allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 19, band 19p13.2 — in an intron of XAB2.

What each result means

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

Questions about rs4134826

What is rs4134826?

rs4134826 is a single position in the genome, in or near the XAB2 gene. Published research associates it with resistin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4134826 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 rs4134826 come from?

GWAS Catalog, Nature metabolism 2020, PMID:33067605. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Resistin levels (rs4134826). MyGeneLog™. https://www.mygenelog.com/variants/rs4134826

← See all variants