rs3093958
This is a regulatory region variant variant in the LINC01149 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.
Myasthenia gravis
Chia R et al. “Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.” Proceedings of the National Academy of Sciences of the United States of America 119(5) (2022)
Allele G
OR 4.49
p 4.0e-42
N 3,313
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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