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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 350,474 European ancestry individuals, 152,447 East Asian ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0156 lower (95% confidence interval 0.012-0.019); p = 5 × 10−16.
Where it sits Chromosome 15, band 15q24.1 — in an intron of SCAMP2.
What each result means
C/CNo copy of the version the research linked to Hemoglobin. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Hemoglobin. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Hemoglobin. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs6495124 is a single position in the genome, in or near the SCAMP2 gene. Published research associates it with hemoglobin. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6495124 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 rs6495124 come from?
GWAS Catalog, Nature genetics 2021, PMID:34594039. 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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