SCN10A · rs112718371
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 1,386 European ancestry individuals, 56 individuals.
The effect Each copy of the T allele shifted the measure 17.8 lower (95% confidence interval 11.42-24.16); p = 5 × 10−8.
How common The T allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 3, band 3p22.2 — in an intron of SCN10A.
rs112718371 is a single position in the genome, in or near the SCN10A gene. Published research associates it with physical health related quality of life. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, Cancers (Basel) 2021, PMID:33578652. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.