rs113851554

GWAS Catalog Trait Associations (11)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

movement disorder

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 G
OR 0.63
p 1.0e-200
N 435,255
Major Consortium StudyLarge GWAS
European

Sleep Disorder

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 G
OR 0.20
p 2.0e-65
N 393,565
Major Consortium StudyLarge GWAS
European

insomnia measurement

Allele T
OR 1.23
p 2.0e-51
N 1,331,010
Large GWAS
European
Lane JM et al. Biological and clinical insights from genetics of insomnia symptoms. Nature Genetics 51(3):387-393 (2019)
Allele T
OR 1.14
p 1.0e-29
N 453,379
Large GWAS
European

extrapyramidal and movement disease

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 G
OR 0.21
p 3.0e-21
N 436,411
Major Consortium StudyLarge GWAS
European

sleep duration trait

Allele G
OR 0.09
p 3.0e-18
N 91,105
Large GWAS
European

chronotype measurement

Allele G
OR 1.06
p 2.0e-13
N 403,195
Large GWAS
European
Allele G
OR 0.03
p 1.0e-8
N 434,835
Large GWAS
European

periodic limb movement disorder

Allele T
OR 1.63
p 4.0e-12
N 6,843
Large GWAS
European, African unspecified, East Asian, Native American

insomnia

Allele T
OR
p 1.0e-21
N 422,239
Large GWAS
multi-ancestry
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 T
OR 0.10
p 4.0e-15
N 408,138
Major Consortium StudyLarge GWAS
European
Allele T
OR 8.94
p 4.0e-19
N 113,006
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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