rs2289002

This is a intron variant variant in the PROX1 gene.

GWAS Catalog Trait Associations (4)

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

erythrocyte count

Allele T
OR 0.02
p 2.0e-57
N 928,679
Large GWAS
multi-ancestry
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 T
OR 0.03
p 7.0e-24
N 405,366
Major Consortium StudyLarge GWAS
European

hematocrit

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 0.03
p 7.0e-65
N 503,490
Large GWAS
multi-ancestry
Allele C
OR 0.03
p 4.0e-14
N 142,940
Large GWAS
East Asian

red blood cell density

Allele C
OR 0.03
p 5.0e-12
N 150,708
Large GWAS
East Asian

hemoglobin measurement

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 C
OR 0.02
p 1.0e-15
N 407,894
Major Consortium StudyLarge GWAS
European
Allele C
OR 0.03
p 6.0e-13
N 149,861
Large GWAS
East Asian

About PROX1

The protein encoded by this gene is a member of the homeobox transcription factor family. Members of this family contain a homeobox domain that consists of a 60-amino acid helix-turn-helix structure that binds DNA and RNA. The protein encoded by this gene is conserved across vertebrates and may play an essential role during development. Altered levels of this protein have been reported in cancers of different organs, such as colon, brain, blood, breast, pancreas, liver and esophagus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]

View all PROX1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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