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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 162,774 Icelandic ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.03 lower (95% confidence interval 0.04-0.02); p = 1 × 10−9.
How common The T allele had a frequency of about 27% in the people studied.
Where it sits Chromosome 12, band 12p13.32 — in an intron of RAD51AP1.
What each result means
C/CNo copy of the version the research linked to Serum alkaline phosphatase levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Serum alkaline phosphatase levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Serum alkaline phosphatase levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
Questions about rs10849087
What is rs10849087?
rs10849087 is a single position in the genome, in or near the C12orf4 gene. Published research associates it with serum alkaline phosphatase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10849087 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 rs10849087 come from?
GWAS Catalog, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020, PMID:31666285. 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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