rs4690221

This variant is located in the SLC26A1 gene.

GWAS Catalog Trait Associations (1)

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

Alzheimer disease

Lake J et al. Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease. Molecular Psychiatry 28(7):3121-3132 (2023)
Allele T
OR
p 4.0e-8
N 644,188
Meta-analysisLarge GWAS
multi-ancestry

ClinVar annotation

Benign★★★
4 submitters2 publications

not provided; not specified

View on ClinVar →

Research that mentions this SNP (1)

Identification of candidate genes carrying polymorphisms associated with the risk of colorectal cancer by analyzing the colorectal mutome and microRNAome
FunctionalN=23Debora Landi et al.(2012)· Cancer

Bioinformatics analysis of exome sequencing data from 23 colorectal cancer patients treated with Cetuximab to identify candidate genes explaining differential skin rash response. Using a novel Molecular Systems Map approach, the study identified 12 candidate genes (C3, CCNK, CD86, CDH11, COL4A4, GRIP2, NUP210, P3H3, STUB1, TLR5, KISS1, ERMAP) with variants potentially affecting EGFR signaling, immune response, and cell adhesion pathways.

Traits studied:Cetuximab-induced skin rash in colorectal cancer

About SLC26A1

This gene is a member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures, but have markedly different tissue expression patterns. This gene is primarily expressed in the liver, pancreas, and brain. Three splice variants that encode different isoforms have been identified. [provided by RefSeq, Jul 2008]

View all SLC26A1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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