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Who was studied 720 African American or Afro-Caribbean cases, 119,025 African American or Afro-Caribbean controls, 2,161 European ancestry cases, 441,880 European ancestry controls, 232 Hispanic or Latin American cases, 58,997 Hispanic or Latin American controls.
The effect
Each copy of the T allele shifted the measure 3.36 lower (95% confidence interval 3.34-3.38); p = 4 × 10−11.
How common The T allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 12, band 12p12.1 — in an intron of SLCO1B1.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Pulmonary congestion and hypostasis (PheCode 503) — no copies of the reported risk allele.
A/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pulmonary congestion and hypostasis (PheCode 503).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pulmonary congestion and hypostasis (PheCode 503) compared to the general population.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs142957626
What is rs142957626?
rs142957626 is a single position in the genome, in or near the SLCO1B1 gene. Published research associates it with pulmonary congestion and hypostasis (phecode 503). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs142957626 affect how medicines work?
SLCO1B1 carries pharmacogenomic findings for Statins, Ticagrelor. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
Does having rs142957626 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 rs142957626 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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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.
Pulmonary congestion and hypostasis (PheCode 503) (rs142957626). MyGeneLog™. https://www.mygenelog.com/variants/rs142957626