rs6564907

This is a intron variant variant in the CMIP gene.

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GWAS Catalog Trait Associations (1)

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

protein measurement

He B et al. “Genome-wide pQTL analysis of protein expression regulatory networks in the human liver.” Bmc Biology 18(1):97 (2020)

Allele C

OR —

β 0.020

p 9.0e-11

N 287

Small GWAS

multi-ancestry

About CMIP

This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

View all CMIP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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