rs5398
This variant is located in the SLC2A2 gene.
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
amount of hepatocyte growth factor receptor (human) in blood
cholesteryl esters to total lipids in large HDL percentage
cholesterol to total lipids in large LDL percentage
discoidin, CUB and LCCL domain-containing protein 2 measurement
phospholipids:total lipids ratio
▶ClinVar annotation
not specified; Fanconi-Bickel syndrome; not provided; Type 2 diabetes mellitus
View on ClinVar →About SLC2A2
This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]
View all SLC2A2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…