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Lysophosphatidylethanolamine_22:4_[M-H]1- levels

RAB3IL1 · rs174478

What the study found

Who was studied 13,814 British ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.152 higher (95% confidence interval 0.13-0.17); p = 1 × 10−57.

Where it sits Chromosome 11, band 11q12.3 — in an intron of RAB3IL1.

What each result means

G/G Two copies of the version the research linked to Lysophosphatidylethanolamine_22:4_[M-H]1- levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/T One copy of the version the research linked to Lysophosphatidylethanolamine_22:4_[M-H]1- levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Lysophosphatidylethanolamine_22:4_[M-H]1- levels. This is the starting point the study compared everyone against.
Source

Questions about rs174478

What is rs174478?

rs174478 is a single position in the genome, in or near the RAB3IL1 gene. Published research associates it with lysophosphatidylethanolamine_22:4_[m-h]1- levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs174478 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 rs174478 come from?

GWAS Catalog, BMC medicine 2021, PMID:34503513. 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.

Lysophosphatidylethanolamine_22:4_[M-H]1- levels (rs174478). MyGeneLog™. https://www.mygenelog.com/variants/rs174478

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