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Rosacea symptom severity

ZBTB12 · rs519417

Where this position leads

Condition: Rosacea

rs519417 Condition: Rosacea Rosacea Condition rs519417 rs519417 ZBTB12

What the study found

Who was studied 73,265 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.208 higher (95% confidence interval 0.15-0.27); p = 7 × 10−11.

Where it sits Chromosome 6, band 6p21.33 — in an intron of C2.

What each result means

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

Questions about rs519417

What is rs519417?

rs519417 is a single position in the genome, in or near the ZBTB12 gene. Published research associates it with rosacea symptom severity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs519417 linked to?

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

Does having rs519417 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 rs519417 come from?

GWAS Catalog, Hum Mol Genet 2018, PMID:29771307. 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.

Rosacea symptom severity (rs519417). MyGeneLog™. https://www.mygenelog.com/variants/rs519417

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