rs4920605

GWAS Catalog Trait Associations (9)

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

brain attribute

van der Meer D et al. The genetic architecture of human cortical folding. Science Advances 7(51):eabj9446 (2021)
Allele G
OR 14.60
p 3.0e-48
N 33,748
Large GWAS
European

cerebral cortex area attribute

van der Meer D et al. The genetic architecture of human cortical folding. Science Advances 7(51):eabj9446 (2021)
Allele G
OR 10.67
p 1.0e-26
N 33,748
Large GWAS
European
Allele G
OR
p 1.0e-17
N 35,657
Large GWAS
European

BMI-adjusted hip circumference

Allele G
OR 0.03
p 2.0e-25
N 186,825
Major Consortium StudyLarge GWAS
European
Tachmazidou I et al. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. American Journal of Human Genetics 100(6):865-884 (2017)
Allele G
OR 0.05
p 2.0e-9
N 36,917
Large GWAS
European

blood protein amount

Allele G
OR 0.18
p 3.0e-22
N 5,365
Large GWAS
European

BMI-adjusted waist circumference

Allele G
OR 0.03
p 3.0e-18
N 186,825
Major Consortium StudyLarge GWAS
European
Tachmazidou I et al. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. American Journal of Human Genetics 100(6):865-884 (2017)
Allele G
OR 0.04
p 4.0e-8
N 50,145
Large GWAS
European

forced expiratory volume

Allele G
OR 0.01
p 9.0e-16
N 373,397
Large GWAS
European

Abnormality of the skeletal system

Allele A
OR 0.01
p 2.0e-14
N 394,642
Large GWAS
European

microfibrillar-associated protein 2 measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.38
p 2.0e-180
N 10,708
Large GWAS
European
Sun BB et al. Genomic atlas of the human plasma proteome. Nature 558(7708):73-79 (2018)
Allele A
OR 0.21
p 1.0e-17
N 3,301
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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