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Progesterone levels

KCNH1 · rs79589801

What the study found

Who was studied 1,358 European ancestry men, 1,261 European ancestry women.

The effect Each copy of the T allele shifted the measure 0.808 higher (95% confidence interval 0.53-1.09); p = 2 × 10−8.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 1, band 1q32.2 — in an intron of KCNH1.

What each result means

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

Questions about rs79589801

What is rs79589801?

rs79589801 is a single position in the genome, in or near the KCNH1 gene. Published research associates it with progesterone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs79589801 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 rs79589801 come from?

GWAS Catalog, The Journal of clinical endocrinology and metabolism 2019, PMID:31169883. 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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Progesterone levels (rs79589801). MyGeneLog™. https://www.mygenelog.com/variants/rs79589801

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