Standard

Glucose (fasting status unknown, mean, inv-norm transformed)

PSMA1 · rs75336838

What the study found

Who was studied 419,946 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.112 lower (95% confidence interval 0.092-0.132); p = 4 × 10−27.

How common The C allele had a frequency of about 98% in the people studied.

Where it sits Chromosome 11, band 11p15.2 — in a regulatory region of PSMA1.

What each result means

C/C Two copies of the version the research linked to Glucose (fasting status unknown, mean, inv-norm transformed). 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 Glucose (fasting status unknown, mean, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to Glucose (fasting status unknown, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs75336838

What is rs75336838?

rs75336838 is a single position in the genome, in or near the PSMA1 gene. Published research associates it with glucose (fasting status unknown, mean, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs75336838 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 rs75336838 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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Glucose (fasting status unknown, mean, inv-norm transformed) (rs75336838). MyGeneLog™. https://www.mygenelog.com/variants/rs75336838

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