Standard

Atopic dermatitis

near CCDST · rs144881827

Where this position leads

Condition: Atopic Dermatitis

rs144881827 Condition: Atopic Dermatitis Atopic Dermatitis Condition rs144881827 rs144881827 near CCDST

What the study found

Who was studied 33,262 European ancestry cases, 804,234 European ancestry controls; replicated in 7,267 East Asian ancestry cases, 219,529 East Asian ancestry controls, 2,785 African American or Afro-Caribbean cases, 3,933 African American or Afro-Caribbean controls.

The effect Each copy of the T allele shifted the measure 0.132 higher (95% confidence interval 0.1-0.16); p = 7 × 10−18.

Where it sits Chromosome 1, band 1q21.3 — between genes, 27.2 kb from CCDST.

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 rs144881827

What is rs144881827?

rs144881827 is a single position in the genome, in or near the near CCDST 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 rs144881827 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 rs144881827 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 rs144881827 come from?

GWAS Catalog, The Journal of investigative dermatology 2022, PMID:35577104. 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 (rs144881827). MyGeneLog™. https://www.mygenelog.com/variants/rs144881827

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