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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 10,708 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.103 lower (95% confidence interval 0.076-0.13); p = 1 × 10−13.
How common The A allele had a frequency of about 70% in the people studied.
Where it sits Chromosome 7, band 7p14.3 — in an intron of NT5C3A.
What each result means
A/ATwo copies of the version the research linked to Cytosolic 5-nucleotidase 3A 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 Cytosolic 5-nucleotidase 3A levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Cytosolic 5-nucleotidase 3A levels. This is the starting point the study compared everyone against.
rs7798138 is a single position in the genome, in or near the NT5C3A gene. Published research associates it with cytosolic 5-nucleotidase 3a levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7798138 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 rs7798138 come from?
GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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