Thyroid stimulating hormone levels within normal range in pregnancy
LINC02454 · rs12321067
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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 67,471 Chinese ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0777 lower (95% confidence interval 0.058-0.098); p = 3 × 10−14.
How common The C allele had a frequency of about 12% in the people studied.
Where it sits Chromosome 12, band 12q14.3 — in an intron of LINC02454.
What each result means
C/CTwo copies of the version the research linked to Thyroid stimulating hormone levels within normal range in pregnancy. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Thyroid stimulating hormone levels within normal range in pregnancy. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Thyroid stimulating hormone levels within normal range in pregnancy. This is the starting point the study compared everyone against.
Nature communications · 2024 · PMID 39266554 · open access
Questions about rs12321067
What is rs12321067?
rs12321067 is a single position in the genome, in or near the LINC02454 gene. Published research associates it with thyroid stimulating hormone levels within normal range 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 rs12321067 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 rs12321067 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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Thyroid stimulating hormone levels within normal range in pregnancy (rs12321067). MyGeneLog™. https://www.mygenelog.com/variants/rs12321067