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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 3,427 Chinese ancestry individuals, 1,735 Malay ancestry individuals, 1,520 Asian Indian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.362 lower (95% confidence interval 0.29-0.43); p = 1 × 10−24.
How common The G allele had a frequency of about 3% in the people studied.
Where it sits Chromosome 17, band 17q21.31 — in an intron of ASB16-AS1.
What each result means
G/GTwo copies of the version the research linked to Glycated hemoglobin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Glycated hemoglobin levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Glycated hemoglobin levels. This is the starting point the study compared everyone against.
rs12602486 is a single position in the genome, in or near the G6PC3 gene. Published research associates it with glycated hemoglobin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12602486 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 rs12602486 come from?
GWAS Catalog, PloS one 2013, PMID:24244560. 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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