rs174529
This variant is located in the MYRF gene.
▶GWAS Catalog Trait Associations (35)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (35)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
phosphatidylcholine (18:0/20:2, 20:0/18:2) measurement
triglycerides in very large VLDL measurement
blood VLDL cholesterol amount
total lipids in very large VLDL measurement
free cholesterol in large VLDL measurement
lysophosphatidylcholine 22:5 measurement
total lipids in medium VLDL
free cholesterol in medium VLDL measurement
triglyceride measurement, blood VLDL cholesterol amount, chylomicron amount
total cholesterol in large VLDL
▶ClinVar annotation
About MYRF
This gene encodes a transcription factor that is required for central nervous system myelination and may regulate oligodendrocyte differentiation. It is thought to act by increasing the expression of genes that effect myelin production but may also directly promote myelin gene expression. Loss of a similar gene in mouse models results in severe demyelination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
View all MYRF variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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