rs9271588
This is a regulatory region variant variant.
▶GWAS Catalog Trait Associations (8)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (8)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
myeloid leukocyte count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.06
p 9.0e-68
N 169,219
Large GWAS
European
granulocyte count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.06
p 2.0e-66
N 169,822
Large GWAS
European
neutrophil count, eosinophil count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.06
p 4.0e-66
N 170,384
Large GWAS
European
neutrophil count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.06
p 1.0e-58
N 170,702
Large GWAS
European
neutrophil count, basophil count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.06
p 2.0e-58
N 170,143
Large GWAS
European
Sjogren syndrome
Li Y et al. “A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.” Nature Genetics 45(11):1361-5 (2013)
Allele T
OR 1.75
p 9.0e-37
N 1,592
Large GWAS
East Asian
wheat allergic reaction
Noguchi E et al. “HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy.” The Journal of Allergy and Clinical Immunology 144(5):1354-1363 (2019)
Allele G
OR 2.30
p 1.0e-26
N 3,152
Large GWAS
East Asian
extranodal nasal NK/T cell lymphoma
Lin GW et al. “Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study in multiple populations.” The Lancet. Oncology 21(2):306-316 (2020)
Allele C
OR 1.53
p 9.0e-26
N 8,452
Large GWAS
East Asian
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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