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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 1,338 Japanese ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.33 lower (95% confidence interval 0.25-0.41); p = 1 × 10−19.
How common The A allele had a frequency of about 36% in the people studied.
Where it sits Chromosome 7, band 7p11.2 — in an intron of ZNF713.
What each result means
A/ATwo copies of the version the research linked to Plasma free amino acid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Plasma free amino acid levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Plasma free amino acid levels. This is the starting point the study compared everyone against.
European journal of human genetics : EJHG · 2019 · PMID 30659259 · open access
Questions about rs2135116
What is rs2135116?
rs2135116 is a single position in the genome, in or near the ZNF713 gene. Published research associates it with plasma free amino acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2135116 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 rs2135116 come from?
GWAS Catalog, European journal of human genetics : EJHG 2019, PMID:30659259. 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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