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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 7,550 European ancestry individuals; replicated in 8,790 European ancestry individuals, 2,030 African American individuals.
The effect
Each copy of the G allele shifted the measure 7.21 z-score lower; p = 6 × 10−13.
How common The G allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 22, band 22q12.3 — in an intron of LINC02558.
What each result means
A/ANo copy of the version the research linked to 1,5-anhydroglucitol levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to 1,5-anhydroglucitol levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to 1,5-anhydroglucitol levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Scientific reports · 2017 · PMID 28588231 · open access
Questions about rs117086479
What is rs117086479?
rs117086479 is a single position in the genome, in or near the SLC5A1 gene. Published research associates it with 1,5-anhydroglucitol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117086479 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 rs117086479 come from?
GWAS Catalog, Scientific reports 2017, PMID:28588231. 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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