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Free thyroxine levels within normal range in pregnancy

near SGF29 · rs76569227

What the study found

Who was studied 67,315 Chinese ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0568 higher (95% confidence interval 0.042-0.072); p = 2 × 10−13.

How common The T allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 16, band 16p11.2 — between genes, 0.2 kb from SGF29.

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 rs76569227

What is rs76569227?

rs76569227 is a single position in the genome, in or near the near SGF29 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 rs76569227 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 rs76569227 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

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Free thyroxine levels within normal range in pregnancy (rs76569227). MyGeneLog™. https://www.mygenelog.com/variants/rs76569227

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