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X-12847 levels

SLC17A1 · rs942377

What the study found

Who was studied 8,809 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.152 higher (95% confidence interval 0.12-0.19); p = 1 × 10−17.

Where it sits Chromosome 6, band 6p22.2 — in an intron of SLC17A1.

What each result means

C/C Two copies of the version the research linked to X-12847 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 X-12847 levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to X-12847 levels. This is the starting point the study compared everyone against.
Source

Questions about rs942377

What is rs942377?

rs942377 is a single position in the genome, in or near the SLC17A1 gene. Published research associates it with x-12847 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs942377 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 rs942377 come from?

GWAS Catalog, Metabolites 2022, PMID:35050183. 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.

X-12847 levels (rs942377). MyGeneLog™. https://www.mygenelog.com/variants/rs942377

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