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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 21,758 European ancestry individuals; replicated in 9,173 individuals.
The effect
Each copy of the T allele shifted the measure 0.108 higher; p = 2 × 10−16.
How common The T allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 1, band 1q31.3 — in an intron of CFH.
What each result means
C/CNo copy of the version the research linked to TNF-related apoptosis-inducing ligand levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to TNF-related apoptosis-inducing ligand levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to TNF-related apoptosis-inducing ligand levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs35617250 is a single position in the genome, in or near the CFH gene. Published research associates it with tnf-related apoptosis-inducing ligand levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35617250 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 rs35617250 come from?
GWAS Catalog, Nature metabolism 2020, PMID:33067605. 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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