rs312691
This is a intron variant variant.
▶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.
Graves disease, thyrotoxic periodic paralysis
Zhao SX et al. “Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.” Jama Network Open 2(5):e193348 (2019)
Allele C
OR 2.02
p 6.0e-24
N 2,331
Large GWAS
East Asian
thyrotoxic periodic paralysis
Cheung CL et al. “Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.” Nature Genetics 44(9):1026-9 (2012)
Allele C
OR 3.20
p 8.0e-14
N 1,239
Large GWAS
East Asian
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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