Standard

Atopic dermatitis

near KPLCE · rs61812715

Where this position leads

Condition: Atopic Dermatitis

rs61812715 Condition: Atopic Dermatitis Atopic Dermatitis Condition rs61812715 rs61812715 near KPLCE

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 0.5 lower (95% confidence interval 0.42-0.58); p = 3 × 10−32.

Where it sits Chromosome 1, band 1q21.3 — between genes, 1 kb from LCEP2.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Atopic dermatitis — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Atopic dermatitis.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Atopic dermatitis compared to the general population.
Source

Questions about rs61812715

What is rs61812715?

rs61812715 is a single position in the genome, in or near the near KPLCE 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 rs61812715 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 rs61812715 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 rs61812715 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 (rs61812715). MyGeneLog™. https://www.mygenelog.com/variants/rs61812715

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