rs11694902

This is a intron variant variant in the TFCP2L1 gene.

GWAS Catalog Trait Associations (4)

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

hemoglobin measurement

Allele A
OR 0.03
p 5.0e-27
N 563,946
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 A
OR 0.03
p 1.0e-23
N 408,112
Large GWAS
European

glomerular filtration rate

Allele G
OR 0.00
p 1.0e-25
N 1,004,040
Large GWAS
European
Allele G
OR 0.00
p 2.0e-20
N 765,348
Large GWAS
multi-ancestry

red blood cell density

Allele A
OR 0.03
p 1.0e-21
N 545,203
Large GWAS
European

hematocrit

Allele A
OR
p 8.0e-26
N 737,823
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.03
p 4.0e-25
N 408,112
Large GWAS
European

About TFCP2L1

Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

View all TFCP2L1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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