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Thyroid stimulating hormone levels

PDE10A · rs73022105

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 0.0823 higher (95% confidence interval 0.069-0.095); p = 7 × 10−35.

How common The T allele had a frequency of about 96% in the people studied.

Where it sits Chromosome 6, band 6q27 — in an intron of PDE10A.

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 rs73022105

What is rs73022105?

rs73022105 is a single position in the genome, in or near the PDE10A 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 rs73022105 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 rs73022105 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 (rs73022105). MyGeneLog™. https://www.mygenelog.com/variants/rs73022105

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