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Facial morphology (multitrait analysis)

near KCTD15 · rs3810361

What the study found

Who was studied 10,115 European ancestry individuals; replicated in 3,948 European ancestry individuals, 9,674 Chinese ancestry individuals.

The effect The reported allele is T; the catalogue records no effect size ; p = 4 × 10−28.

How common The T allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 19, band 19q13.11 — between genes, 0.9 kb from KCTD15.

What each result means

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

Questions about rs3810361

What is rs3810361?

rs3810361 is a single position in the genome, in or near the near KCTD15 gene. Published research associates it with facial morphology (multitrait analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3810361 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 rs3810361 come from?

GWAS Catalog, Nature communications 2022, PMID:36539420. 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.

Facial morphology (multitrait analysis) (rs3810361). MyGeneLog™. https://www.mygenelog.com/variants/rs3810361

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