rs80051818
This variant is located in the EIF2B4 gene.
▶GWAS Catalog Trait Associations (17)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (17)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
triglyceride measurement
C-reactive protein measurement
sex hormone-binding globulin measurement
serum gamma-glutamyl transferase measurement
urate measurement
serum albumin amount
total cholesterol measurement
IGF-1 measurement
apolipoprotein B measurement
low density lipoprotein cholesterol measurement
▶ClinVar annotation
About EIF2B4
Eukaryotic initiation factor 2B (EIF2B), which is necessary for protein synthesis, is a GTP exchange factor composed of five different subunits. The protein encoded by this gene is the fourth, or delta, subunit. Defects in this gene are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
View all EIF2B4 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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