rs6138584
This is a intron variant variant in the NINL gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
urate measurement
Tin A et al. “Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.” Nature Genetics 51(10):1459-1474 (2019)
Allele A
OR 0.02
p 3.0e-9
N 457,690
Large GWAS
multi-ancestry
About NINL
Predicted to enable calcium ion binding activity. Predicted to be involved in microtubule anchoring at centrosome. Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]
View all NINL variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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