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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 4,845 European ancestry individuals from 2,892 families, 16,140 European ancestry individuals.
The effect
The reported allele is T; the catalogue records no effect size
; p = 2 × 10−8.
Where it sits Chromosome 1, band 1q21.3 — between genes, 13 kb from THEM4.
What each result means
C/CNo copy of the version the research linked to Hair morphology. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Hair morphology. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Hair morphology. That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of human genetics · 2009 · PMID 19896111
Questions about rs10788819
What is rs10788819?
rs10788819 is a single position in the genome, in or near the AL450992.4 gene. Published research associates it with hair morphology. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10788819 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 rs10788819 come from?
GWAS Catalog, American journal of human genetics 2009, PMID:19896111. 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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