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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 4,988 Spanish ancestry individuals; replicated in 336,107 British ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0342 higher (95% confidence interval 0.03-0.038); p = 3 × 10−67.
How common The G allele had a frequency of about 26% in the people studied.
Where it sits Chromosome 5, band 5q35.3 — in an intron of MXD3.
What each result means
A/ANo copy of the version the research linked to Anthropometric traits. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Anthropometric traits. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Anthropometric traits. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of medical genetics · 2018 · PMID 30166351 · open access
Questions about rs111251222
What is rs111251222?
rs111251222 is a single position in the genome, in or near the PRELID1 gene. Published research associates it with anthropometric traits. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs111251222 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 rs111251222 come from?
GWAS Catalog, J Med Genet 2018, PMID:30166351. 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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