rs72932727
This is a intron variant variant in the ICA1L 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.
non-lobar intracerebral hemorrhage
Chung J et al. “Genome-wide association study of cerebral small vessel disease reveals established and novel loci.” Brain : a Journal of Neurology 142(10):3176-3189 (2019)
Allele G
OR 1.11
p 2.0e-8
N 2,716
Large GWAS
European
About ICA1L
Predicted to enable protein domain specific binding activity. Predicted to be involved in regulation of transport. Predicted to act upstream of or within spermatid development. Predicted to be located in acrosomal vesicle. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
View all ICA1L variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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