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Vitiligo

BCL2L11 · rs4308124

Where this position leads

Condition: Vitiligo

rs4308124 Condition: Vitiligo Vitiligo Condition rs4308124 rs4308124 BCL2L11

What the study found

Who was studied 2,853 European ancestry cases and 37,405 European ancestry controls; replicated in 1,827 European ancestry cases and 2,181 European ancestry controls.

The effect Each copy of the C allele carried 1.15 times the odds of Vitiligo (95% confidence interval 1.10-1.21); p = 4 × 10−9.

How common The C allele had a frequency of about 41% in the people studied.

Where it sits Chromosome 2, band 2q13 — in an intron of MIR4435-2HG.

What each result means

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

Questions about rs4308124

What is rs4308124?

rs4308124 is a single position in the genome, in or near the BCL2L11 gene. Published research associates it with vitiligo. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4308124 linked to?

On MyGeneLog this position is linked to Vitiligo. The research behind each link, and its sources, are set out on that condition page.

Does having rs4308124 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 rs4308124 come from?

GWAS Catalog, Nat Genet 2016, PMID:27723757. 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.

Vitiligo (rs4308124). MyGeneLog™. https://www.mygenelog.com/variants/rs4308124

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