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17-hydroxyprogesterone (17-OHP) levels

MDC1 · rs115448006

What the study found

Who was studied 1,358 European ancestry men, 712 European ancestry women.

The effect Each copy of the T allele shifted the measure 0.6 higher (95% confidence interval 0.42-0.78); p = 5 × 10−11.

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

Where it sits Chromosome 6, band 6p21.33 — in an intron of MDC1.

What each result means

G/G No copy of the version the research linked to 17-hydroxyprogesterone (17-OHP) levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to 17-hydroxyprogesterone (17-OHP) levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to 17-hydroxyprogesterone (17-OHP) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs115448006

What is rs115448006?

rs115448006 is a single position in the genome, in or near the MDC1 gene. Published research associates it with 17-hydroxyprogesterone (17-ohp) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs115448006 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 rs115448006 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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17-hydroxyprogesterone (17-OHP) levels (rs115448006). MyGeneLog™. https://www.mygenelog.com/variants/rs115448006

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