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Total testosterone levels

RNF19A · rs1660322

What the study found

Who was studied 230,454 European ancestry women.

The effect Each copy of the T allele shifted the measure 0.0233 higher (95% confidence interval 0.017-0.029); p = 5 × 10−15.

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

Where it sits Chromosome 8, band 8q22.2 — in an intron of RNF19A.

What each result means

C/C No copy of the version the research linked to Total testosterone levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Total testosterone levels. That is a smaller link than two copies.
T/T 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.
Source

Questions about rs1660322

What is rs1660322?

rs1660322 is a single position in the genome, in or near the RNF19A 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 rs1660322 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 rs1660322 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

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Total testosterone levels (rs1660322). MyGeneLog™. https://www.mygenelog.com/variants/rs1660322

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