rs10028213
This is a intergenic variant variant in the LOC107986195 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
hypothyroidism
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.10
p 5.0e-35
N 626,668
Major Consortium StudyLarge GWAS
multi-ancestry
thyroid function
Rawal R et al. “Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.” Human Molecular Genetics 21(14):3275-82 (2012)
Allele C
OR 0.08
p 3.0e-10
N 3,736
Meta-analysis
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…