rs11264341
This variant is located in the TRIM46 gene.
▶GWAS Catalog Trait Associations (11)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (11)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
uric acid measurement
serum urea amount
urate measurement
gout
serum gamma-glutamyl transferase measurement
drug use measurement, gout
calcium measurement
serum alanine aminotransferase amount
aspartate aminotransferase measurement
blood phosphate measurement
▶Research that mentions this SNP (1)
▶Epigenetic and genetic variation in GATA5 is associated with gastric disease riskAssociationN=289Sobota RS et al.(2016)· Human Genetics
A discovery and replication study of 130 and 159 Colombian patients examining genetic and epigenetic variation in GATA5 associated with gastric disease progression. Two synonymous SNPs in GATA5 (rs6061243 and rs6587239) were significantly associated with histopathology scores in dominant-effect models (p = 2.63×10⁻⁷ and 7.97×10⁻⁷, respectively, β = -0.86 and -0.82) and replicated in additive/dominant models. GATA5 promoter methylation was independently associated with disease progression (p = 0.001), and a significant SNP-by-methylation interaction indicated non-linear combined effects on gastric lesion severity.
About TRIM46
This gene encodes a protein of the tripartite motif (TRIM) family. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. TRIM46 is reported to be involved in the proliferation of multiple types of cancer cells including lung and breast cancer. It has also been shown to control neuronal polarity and axon specification by forming uniform microtubule bundles in the axon. [provided by RefSeq, May 2022]
View all TRIM46 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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