rs2989476
This is a intron variant variant in the LINC01748 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.
self reported educational attainment
▶Research that mentions this SNP (1)
▶Propensity score‐based nonparametric test revealing genetic variants underlying bipolar disorderMethodsN=5,002Yuan Jiang et al.(2011)· Genetic Epidemiology
This methods paper presents a propensity score-based nonparametric test for genetic association that adjusts for covariates using genomic propensity scores. Applied to 1,998 bipolar disorder cases and 3,004 controls from the Wellcome Trust Case Control Consortium, the method identified three SNPs on chromosome 16 (rs2387823, rs1344485, rs11647459; p < 5×10⁻⁷) in strong linkage disequilibrium near RPGRIP1L that were missed by standard unadjusted methods, demonstrating that covariate-adjusted approaches can reveal genetic variants underlying bipolar disorder.
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…