rs72813970
This is a intron variant variant in the LINC01122 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.
depressive symptom measurement
Thorp JG et al. “Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.” Psychological Medicine 50(14):2385-2396 (2020)
Allele G
OR 0.07
p 6.0e-9
N 148,752
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.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…