rs2737226

This variant is located in the TRPS1 gene.

GWAS Catalog Trait Associations (10)

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

triglycerides to phosphoglycerides ratio

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.02
p 8.0e-23
N 450,015
Large GWAS
multi-ancestry

base metabolic rate measurement

Allele C
OR 0.01
p 1.0e-22
N 394,642
Large GWAS
European

whole body water mass

Allele C
OR 0.01
p 2.0e-22
N 394,642
Large GWAS
European

body weight

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 3.0e-20
N 525,535
Large GWAS
multi-ancestry

type 2 diabetes mellitus

Allele C
OR 0.04
p 3.0e-16
N 1,114,458
Meta-analysisLarge GWAS
European

cholesterol to total lipids in medium HDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.02
p 1.0e-15
N 450,015
Large GWAS
multi-ancestry

triglycerides to total lipids in small HDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.01
p 6.0e-14
N 450,015
Large GWAS
multi-ancestry

triglycerides in large VLDL measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.01
p 2.0e-13
N 450,015
Large GWAS
multi-ancestry

triglyceride:HDL cholesterol ratio

Allele T
OR 0.02
p 2.0e-12
N 402,398
Major Consortium StudyLarge GWAS
European

triglycerides in medium VLDL measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.01
p 6.0e-11
N 450,015
Large GWAS
multi-ancestry

About TRPS1

This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [provided by RefSeq, Jul 2008]

View all TRPS1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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