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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 2,721 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 1.56 lower (95% confidence interval 1.21-1.91); p = 1 × 10−17.
How common The A allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 13, band 13q14.13 — a missense change in LCP1.
What ClinVar records
ClassificationBenign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2019-12-31.
ClinVar record 718752NM_002298.5(LCP1):c.119C>T (p.Ala40Val)
What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
What each result means
A/ATwo copies of the version the research linked to Plastin-2 (analyte X17231.1) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Plastin-2 (analyte X17231.1) levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Plastin-2 (analyte X17231.1) levels. This is the starting point the study compared everyone against.
rs117014375 is a single position in the genome, in or near the LCP1 gene. Published research associates it with plastin-2 (analyte x17231.1) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117014375 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 rs117014375 come from?
GWAS Catalog, Nature genetics 2024, PMID:39528825. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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