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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 6,604 African American or Afro-Caribbean cases, 110,457 African American or Afro-Caribbean controls, 3,015 Hispanic or Latin American cases, 54,613 Hispanic or Latin American controls, 254 East Asian ancestry cases, 6,406 East Asian ancestry controls, 19,418 European ancestry cases, 415,949 European ancestry controls.
The effect
Each copy of the A allele shifted the measure 0.0813 lower (95% confidence interval 0.061-0.102); p = 2 × 10−12.
How common The A allele had a frequency of about 82% in the people studied.
Where it sits Chromosome 8, band 8q24.12 — in an intron of COLEC10.
What each result means
A/ATwo copies of the version the research linked to Microscopic hematuria (PheCode 593.2). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Microscopic hematuria (PheCode 593.2). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Microscopic hematuria (PheCode 593.2). This is the starting point the study compared everyone against.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs7017788
What is rs7017788?
rs7017788 is a single position in the genome, in or near the COLEC10 gene. Published research associates it with microscopic hematuria (phecode 593.2). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7017788 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 rs7017788 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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