rs10445344
This is a intron variant variant in the HLF gene.
▶GWAS Catalog Trait Associations (10)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (10)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
QRS duration
systolic blood pressure
free cholesterol in large HDL measurement
cholesterol in large HDL measurement
cholesteryl esters in large HDL measurement
concentration of large HDL particles measurement
HDL cholesterol change measurement
phospholipids in large HDL measurement
total lipids in large HDL
cholesteryl esters in HDL measurement
About HLF
This gene encodes a member of the proline and acidic-rich (PAR) protein family, a subset of the bZIP transcription factors. The encoded protein forms homodimers or heterodimers with other PAR family members and binds sequence-specific promoter elements to activate transcription. Chromosomal translocations fusing portions of this gene with the E2A gene cause a subset of childhood B-lineage acute lymphoid leukemias. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
View all HLF variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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