rs1905376

This variant is located in the TRPS1 gene.

GWAS Catalog Trait Associations (4)

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

erythrocyte count

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.02
p 6.0e-22
N 503,987
Large GWAS
multi-ancestry
Allele G
OR 0.03
p 1.0e-13
N 172,952
Large GWAS
European

diabetic retinopathy

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.07
p 2.0e-17
N 432,209
Major Consortium StudyLarge GWAS
European

hematocrit

Allele G
OR 0.03
p 6.0e-14
N 173,039
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.04
p 1.0e-11
N 55,841
Major Consortium StudyLarge GWAS
Hispanic or Latin American

blood urea nitrogen amount

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.02
p 5.0e-11
N 598,949
Major Consortium StudyLarge 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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