rs12149643
This is a intron variant variant.
▶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.
cerebral small vessel disease
Mishra A et al. “Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.” Brain : a Journal of Neurology 145(6):1992-2007 (2022)
Allele T
OR 1.19
p 3.0e-9
N 19,721
Large GWAS
European
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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