FAM131C2P · rs2019654
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 7,548 African ancestry, Hispanic, European ancestry, Asian ancestry, unknown ancestry cases, 23,009 African ancestry, Hispanic, European ancestry, Asian ancestry, unknown ancestry controls.
The effect Each copy of the G allele shifted the measure 0.22 higher (95% confidence interval 0.17-0.27); p = 5 × 10−15.
How common The G allele had a frequency of about 36% in the people studied.
Where it sits Chromosome 1, band 1p36.13 — in a non-coding transcript of FAM131C2P.
rs2019654 is a single position in the genome, in or near the FAM131C2P gene. Published research associates it with supranormal left ventricular ejection fraction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, European journal of heart failure 2022, PMID:35278270. 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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Supranormal left ventricular ejection fraction (rs2019654). MyGeneLog™. https://www.mygenelog.com/variants/rs2019654