rs140511699
This is a intron variant variant in the GRHL2 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
tuberculosis
Gelemanović A et al. “Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk.” International Journal of Molecular Sciences 24(8) (2023)
Allele C
OR 1.07
p 2.0e-9
N 4,624
Meta-analysis
European
About GRHL2
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]
View all GRHL2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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