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Total testosterone levels

near HNRNPDP1 · rs146447930

What the study found

Who was studied 194,453 European ancestry men.

The effect Each copy of the C allele shifted the measure 0.0711 higher (95% confidence interval 0.053-0.089); p = 3 × 10−16.

How common The C allele had a frequency of about 99% in the people studied.

Where it sits Chromosome X, band Xq11.2 — between genes, 96.7 kb from HNRNPDP1.

What each result means

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

Questions about rs146447930

What is rs146447930?

rs146447930 is a single position in the genome, in or near the near HNRNPDP1 gene. Published research associates it with total testosterone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs146447930 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 rs146447930 come from?

GWAS Catalog, Nature medicine 2020, PMID:32042192. 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.

Total testosterone levels (rs146447930). MyGeneLog™. https://www.mygenelog.com/variants/rs146447930

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