PLCL1 · rs1147169
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.
rs1147169 is a single position in the genome, in or near the PLCL1 gene. Published research associates it with low high density lipoprotein cholesterol levels. 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, Clin Genet 2016, PMID:26879886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.