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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 13,577 Finnish ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.163 lower; p = 2 × 10−12.
How common The C allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 6, band 6p22.1 — in an intron of POLR1HASP.
What each result means
C/CTwo copies of the version the research linked to Interleukin-1-beta levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Interleukin-1-beta levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Interleukin-1-beta levels. This is the starting point the study compared everyone against.
Journal of medical genetics · 2019 · PMID 31217265 · open access
Questions about rs6917603
What is rs6917603?
rs6917603 is a single position in the genome, in or near the HLA gene. Published research associates it with interleukin-1-beta levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6917603 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 rs6917603 come from?
GWAS Catalog, Journal of medical genetics 2019, PMID:31217265. 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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