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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 3,594 Chinese ancestry cases, 46,813 Chinese ancestry controls.
The effect
Each copy of the T allele carried 1.56 times the odds of Isolated hypothyroxinemia in pregnancy (95% confidence interval 1.36-1.8); p = 5 × 10−10.
How common The T allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 14, band 14q32.31 — between genes, 12.2 kb from LINC00524.
What each result means
C/CNo copy of the version the research linked to Isolated hypothyroxinemia in pregnancy. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Isolated hypothyroxinemia in pregnancy. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Isolated hypothyroxinemia in pregnancy. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39266554 · open access
Questions about rs17100242
What is rs17100242?
rs17100242 is a single position in the genome, in or near the near LINC00524 gene. Published research associates it with isolated hypothyroxinemia in pregnancy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17100242 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 rs17100242 come from?
GWAS Catalog, Nature communications 2024, PMID:39266554. 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.
Isolated hypothyroxinemia in pregnancy (rs17100242). MyGeneLog™. https://www.mygenelog.com/variants/rs17100242