rs4937333

This is a 3 prime utr variant variant in the ETS1 gene.

GWAS Catalog Trait Associations (3)

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

platelet count

Allele C
OR 0.03
p 1.0e-59
N 542,827
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.03
p 9.0e-43
N 408,112
Large GWAS
European
Allele C
OR 0.03
p 6.0e-51
N 394,642
Large GWAS
European
Allele C
OR 0.03
p 6.0e-18
N 166,066
Large GWAS
European
Allele C
OR 0.06
p 2.0e-8
N 72,816
Large GWAS
East Asian

platelet crit

Allele C
OR 0.02
p 1.0e-42
N 394,642
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.02
p 5.0e-14
N 408,112
Large GWAS
European
Allele C
OR 0.03
p 6.0e-17
N 164,339
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

About ETS1

This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]

View all ETS1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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