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Sphingomyelin (d40:0) levels

ZNF594-DT · rs80120324

What the study found

Who was studied 650 Amish individuals; replicated in 847 European American ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.549 lower; p = 3 × 10−10.

How common The C allele had a frequency of about 13% in the people studied.

Where it sits Chromosome 17, band 17p13.2 — inside ZNF594-DT.

What each result means

C/C Two copies of the version the research linked to Sphingomyelin (d40:0) 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 Sphingomyelin (d40:0) levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Sphingomyelin (d40:0) levels. This is the starting point the study compared everyone against.
Source

Questions about rs80120324

What is rs80120324?

rs80120324 is a single position in the genome, in or near the ZNF594-DT gene. Published research associates it with sphingomyelin (d40:0) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs80120324 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 rs80120324 come from?

GWAS Catalog, Communications biology 2022, PMID:35393526. 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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Sphingomyelin (d40:0) levels (rs80120324). MyGeneLog™. https://www.mygenelog.com/variants/rs80120324

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