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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 7,805 Japanese ancestry individuals.
The effect
Each copy of the C allele shifted the measure 30.7 higher (95% confidence interval 21.07-40.27); p = 4 × 10−10.
How common The C allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 14, band 14q31.1 — in an intron of TSHR-AS1.
What each result means
C/CTwo copies of the version the research linked to Urinary albumin excretion. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Urinary albumin excretion. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Urinary albumin excretion. This is the starting point the study compared everyone against.
Clinical and experimental nephrology · 2020 · PMID 32277301 · open access
Questions about rs116622332
What is rs116622332?
rs116622332 is a single position in the genome, in or near the TSHR gene. Published research associates it with urinary albumin excretion. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs116622332 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 rs116622332 come from?
GWAS Catalog, Clinical and experimental nephrology 2020, PMID:32277301. 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.
Urinary albumin excretion (rs116622332). MyGeneLog™. https://www.mygenelog.com/variants/rs116622332