rs1033182

This is a intron variant variant in the ESR1 gene.

Research that mentions this SNP (2)

HLA-DRB1*1501 and Spinal Cord Magnetic Resonance Imaging Lesions in Multiple Sclerosis
AssociationN=95Sombekke MH et al.(2009)· Archives of Neurology

A retrospective association study of 95 Brazilian multiple sclerosis (MS) patients examined HLA alleles and five SNPs (rs4774, rs3087456, rs6897932, rs731236, rs1033182) for associations with MRI lesion load. The HLA-DQA1*04:01 allele was significantly associated with higher lesion load on T2/FLAIR MRI sequences (p=0.02), with 71% of carriers showing above-median lesion load compared to 41% of non-carriers. No significant associations were found between the five SNPs and any MRI features studied.

Traits studied:Black holes (T1 lesions)Enhanced lesionsMRI lesion loadMultiple Sclerosis
Comprehensive evaluation of the estrogen receptor α gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population
AssociationN=1,173Keith L. Keene et al.(2008)· Human Genetics

A comprehensive candidate gene study evaluating 150 SNPs across 476 kb of the ESR1 gene (estrogen receptor alpha) in 577 African American cases with type 2 diabetes and end-stage renal disease (T2DM-ESRD) versus 596 controls. After multiple testing correction, three SNPs remained significant: rs11964281 (promoter, adjusted P=0.0289), rs1569788 (intron 4, adjusted P=0.0278), and rs9340969 (intron 4, adjusted P=0.0467). A novel region in intron 4-intron 6 showed clustering of 23 associated SNPs, suggesting this region may contain functionally relevant polymorphisms for T2DM/diabetic nephropathy susceptibility.

Traits studied:Diabetic nephropathyEnd-stage renal diseaseType 2 diabetes mellitus

About ESR1

This gene encodes an estrogen receptor and ligand-activated transcription factor. The canonical protein contains an N-terminal ligand-independent transactivation domain, a central DNA binding domain, a hinge domain, and a C-terminal ligand-dependent transactivation domain. The protein localizes to the nucleus where it may form either a homodimer or a heterodimer with estrogen receptor 2. The protein encoded by this gene regulates the transcription of many estrogen-inducible genes that play a role in growth, metabolism, sexual development, gestation, and other reproductive functions and is expressed in many non-reproductive tissues. The receptor encoded by this gene plays a key role in breast cancer, endometrial cancer, and osteoporosis. This gene is reported to have dozens of transcript variants due to the use of alternate promoters and alternative splicing, however, the full-length nature of many of these variants remain uncertain. [provided by RefSeq, Jul 2020]

View all ESR1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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