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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 4,680 European ancestry individuals; replicated in 3,566 European ancestry individuals.
The effect
The reported allele is C; the catalogue records no effect size
; p = 2 × 10−34.
How common The C allele had a frequency of about 28% in the people studied.
Where it sits Chromosome 9, band 9q31.3 — between genes, 18 kb from RPL36P14.
What each result means
C/CTwo copies of the version the research linked to Facial morphology (segment 7). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Facial morphology (segment 7). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Facial morphology (segment 7). This is the starting point the study compared everyone against.
Nature genetics · 2021 · PMID 33288918 · open access
Questions about rs1999464
What is rs1999464?
rs1999464 is a single position in the genome, in or near the near RPL36P14 gene. Published research associates it with facial morphology (segment 7). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1999464 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 rs1999464 come from?
GWAS Catalog, Nature genetics 2021, PMID:33288918. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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