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Free thyroxine levels within normal range in pregnancy

FIG4 · rs9398215

What the study found

Who was studied 67,315 Chinese ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0416 lower (95% confidence interval 0.029-0.054); p = 9 × 10−11.

How common The T allele had a frequency of about 20% in the people studied.

Where it sits Chromosome 6, band 6q21 — in an intron of FIG4.

What each result means

C/C No copy of the version the research linked to Free thyroxine levels within normal range in pregnancy. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Free thyroxine levels within normal range in pregnancy. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Free thyroxine levels within normal range in pregnancy. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs9398215

What is rs9398215?

rs9398215 is a single position in the genome, in or near the FIG4 gene. Published research associates it with free thyroxine 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 rs9398215 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 rs9398215 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.

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.

Free thyroxine levels within normal range in pregnancy (rs9398215). MyGeneLog™. https://www.mygenelog.com/variants/rs9398215

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