rs9915940
This variant is located in the SLFN12L 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.
Red cell distribution width
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 2.0e-15
N 408,112
Large GWAS
European
About SLFN12L
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all SLFN12L variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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