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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 241,736 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0286 higher (95% confidence interval 0.02-0.037); p = 8 × 10−11.
How common The T allele had a frequency of about 12% in the people studied.
Where it sits Chromosome 3, band 3p21.31 — between genes, 2.5 kb from TRAIP.
What each result means
C/CNo copy of the version the research linked to Occupational creativity. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Occupational creativity. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Occupational creativity. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs73079014 is a single position in the genome, in or near the near TRAIP gene. Published research associates it with occupational creativity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs73079014 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 rs73079014 come from?
GWAS Catalog, Psychiatry research 2024, PMID:38335777. 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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