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Cerebrospinal fluid trans-4-hydroxyproline levels

SACM1L · rs73060324

What the study found

Who was studied 2,602 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.104 lower (95% confidence interval 0.089-0.119); p = 6 × 10−45.

Where it sits Chromosome 3, band 3p21.31 — in the 3′ untranslated region of SACM1L.

What each result means

G/G No copy of the version the research linked to Cerebrospinal fluid trans-4-hydroxyproline levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Cerebrospinal fluid trans-4-hydroxyproline levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Cerebrospinal fluid trans-4-hydroxyproline levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs73060324

What is rs73060324?

rs73060324 is a single position in the genome, in or near the SACM1L gene. Published research associates it with cerebrospinal fluid trans-4-hydroxyproline levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs73060324 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 rs73060324 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528826. 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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Cerebrospinal fluid trans-4-hydroxyproline levels (rs73060324). MyGeneLog™. https://www.mygenelog.com/variants/rs73060324

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