rs174533

This variant is located in the MYRF gene.

GWAS Catalog Trait Associations (48)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

fatty acid amount

Allele G
OR 0.17
p
N 115,006
Large GWAS
European
Allele G
OR 0.05
p 3.0e-21
N 5,662
Large GWAS
South Asian

triglyceride measurement

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.11
p 9.9e-324
N 391,626
Major Consortium StudyLarge GWAS
European
Allele G
OR 0.05
p 4.0e-21
N 5,662
Large GWAS
South Asian

level of Phosphatidylcholine (16:0_20:4) in blood serum

Allele A
OR 0.60
p 6.0e-295
N 7,174
Large GWAS
European

level of Phosphatidylcholine (17:0_20:4) in blood serum

Allele A
OR 0.54
p 1.0e-235
N 7,106
Large GWAS
European

level of Phosphatidylcholine (16:0_22:5) in blood serum

Allele A
OR 0.41
p 5.0e-135
N 7,172
Large GWAS
European

citrate measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.03
p 2.0e-56
N 450,015
Large GWAS
multi-ancestry

level of Phosphatidylinositol (18:0_20:4) in blood serum

Allele A
OR 0.25
p 3.0e-49
N 7,174
Large GWAS
European

triacylglycerol 56:6 measurement

Allele A
OR 0.23
p 8.0e-43
N 7,151
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

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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