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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 64,962 European ancestry cases, 410,350 European ancestry controls.
The effect
The reported allele is G; the catalogue records no effect size
; p = 2 × 10−10.
Where it sits Chromosome 6, band 6p21.33 — between genes, 7.7 kb from HCG22.
What each result means
A/ANo copy of the version the research linked to Cancer (pleiotropy)(bidirectional). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Cancer (pleiotropy)(bidirectional). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Cancer (pleiotropy)(bidirectional). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2020 · PMID 32887889 · open access
Questions about rs17190106
What is rs17190106?
rs17190106 is a single position in the genome, in or near the near HCG22 gene. Published research associates it with cancer (pleiotropy)(bidirectional). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17190106 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 rs17190106 come from?
GWAS Catalog, Nature communications 2020, PMID:32887889. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Cancer (pleiotropy)(bidirectional) (rs17190106). MyGeneLog™. https://www.mygenelog.com/variants/rs17190106