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Atopic dermatitis

ETS1 · rs7127307

Where this position leads

Condition: Atopic Dermatitis

rs7127307 Condition: Atopic Dermatitis Atopic Dermatitis Condition rs7127307 rs7127307 ETS1

What the study found

Who was studied 18,900 European ancestry cases, 1,472 Japanese ancestry cases, 422 African American cases, 300 Latino cases, 305 cases, 84,166 European ancestry controls, 7,966 Japanese ancestry controls, 844 African American controls, 1,592 Latino controls, 896 controls; replicated in 30,588 European ancestry cases, 459 African American cases, 1,012 Chinese ancestry cases, 226,537 European ancestry controls, 729 African American controls, 1,362 Chinese ancestry controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 1 × 10−20.

How common The C allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 11, band 11q24.3 — in an intron of LOC124902787.

What each result means

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

Questions about rs7127307

What is rs7127307?

rs7127307 is a single position in the genome, in or near the ETS1 gene. Published research associates it with atopic dermatitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7127307 linked to?

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

Does having rs7127307 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 rs7127307 come from?

GWAS Catalog, Nat Genet 2015, PMID:26482879. 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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Atopic dermatitis (rs7127307). MyGeneLog™. https://www.mygenelog.com/variants/rs7127307

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