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Thyroid stimulating hormone levels

FAF1 · rs1398868

What the study found

Who was studied 247,107 European ancestry individuals; replicated in 63,326 European ancestry individuals, 33,171 South Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.035 higher (95% confidence interval 0.03-0.04); p = 7 × 10−36.

How common The T allele had a frequency of about 69% in the people studied.

Where it sits Chromosome 1, band 1p32.3 — in an intron of FAF1.

What each result means

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

Questions about rs1398868

What is rs1398868?

rs1398868 is a single position in the genome, in or near the FAF1 gene. Published research associates it with thyroid stimulating hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1398868 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 rs1398868 come from?

GWAS Catalog, Nature communications 2023, PMID:37872160. 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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Thyroid stimulating hormone levels (rs1398868). MyGeneLog™. https://www.mygenelog.com/variants/rs1398868

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