rs28652618
This variant is located in the PEMT gene.
▶GWAS Catalog Trait Associations (14)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (14)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
cholesterol in chylomicrons and extremely large VLDL measurement
cholesteryl ester measurement
phospholipids in chylomicrons and extremely large VLDL measurement
phospholipids in very large VLDL measurement
total lipids in large VLDL
triglycerides in large VLDL measurement
free cholesterol in chylomicrons and extremely large VLDL measurement
free cholesterol in very large VLDL measurement
concentration of chylomicrons and extremely large VLDL particles measurement
total lipids in chylomicrons and extremely large VLDL measurement
About PEMT
Phosphatidylcholine (PC) is the most abundant mammalian phospholipid. This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. Another distinct synthetic pathway in nucleated cells converts intracellular choline to phosphatidylcholine by a three-step process. The protein isoforms encoded by this gene localize to the endoplasmic reticulum and mitochondria-associated membranes. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012]
View all PEMT variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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