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Facial morphology (multitrait analysis)

PRDM16 · rs10797388

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 = 2 × 10−33.

How common The T allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 1, band 1p36.32 — in an intron of PRDM16.

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 rs10797388

What is rs10797388?

rs10797388 is a single position in the genome, in or near the PRDM16 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 rs10797388 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 rs10797388 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

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Facial morphology (multitrait analysis) (rs10797388). MyGeneLog™. https://www.mygenelog.com/variants/rs10797388

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