Tumor necrosis factor ligand superfamily member 12 levels
near TNFSF12 · rs62059801
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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 982 Scottish ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.351 higher (95% confidence interval 0.24-0.46); p = 1 × 10−10.
How common The T allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 17, band 17p13.1 — between genes, 2.2 kb from TNFSF12.
What each result means
C/CNo copy of the version the research linked to Tumor necrosis factor ligand superfamily member 12 levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Tumor necrosis factor ligand superfamily member 12 levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Tumor necrosis factor ligand superfamily member 12 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Genome medicine · 2020 · PMID 32641083 · open access
Questions about rs62059801
What is rs62059801?
rs62059801 is a single position in the genome, in or near the near TNFSF12 gene. Published research associates it with tumor necrosis factor ligand superfamily member 12 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62059801 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 rs62059801 come from?
GWAS Catalog, Genome medicine 2020, PMID:32641083. 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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