rs1268367147

This variant is located in the GREB1L gene.

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GWAS Catalog Trait Associations (4)

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

1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele G
OR 0.99
p 8.0e-23
N 6,136
Large GWAS
European

1-myristoyl-GPC (14:0) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele G
OR 0.97
p 1.0e-21
N 6,136
Large GWAS
European

2-myristoyl-GPC (14:0) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele G
OR 0.84
p 7.0e-17
N 6,136
Large GWAS
European

About GREB1L

Acts upstream of or within kidney development. Predicted to be located in membrane. Implicated in autosomal dominant nonsyndromic deafness 80 and renal agenesis. [provided by Alliance of Genome Resources, Jul 2025]

View all GREB1L variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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