rs7115242
▶GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
triglyceride measurement
Kulminski AM et al. “Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.” Aging 10(3):492-514 (2018)
Allele T
OR 7.78
p 7.0e-19
N 33,431
Large GWAS
European
Li D et al. “Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.” Genes & Genomics 42(4):393-403 (2020)
Allele T
OR —
β 0.060
p 9.0e-14
N 6,840
Large GWAS
East Asian
sphingomyelin measurement
Harshfield EL et al. “Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci.” Bmc Medicine 19(1):232 (2021)
Allele A
OR 0.13
p 1.0e-10
N 13,814
Large GWAS
European
sterol level
Harshfield EL et al. “Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci.” Bmc Medicine 19(1):232 (2021)
Allele A
OR 0.10
p 3.0e-10
N 13,814
Large GWAS
European
level of Diacylglycerol (18:1_18:1) in blood serum
Tabassum R et al. “Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids.” Journal of the American Heart Association 11(19):e027103 (2022)
Allele A
OR 0.20
p 2.0e-9
N 4,642
Large GWAS
European
triacylglycerol 52:2 measurement
Tabassum R et al. “Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids.” Journal of the American Heart Association 11(19):e027103 (2022)
Allele A
OR 0.18
p 1.0e-8
N 4,642
Large GWAS
European
metabolic syndrome
Ho CY et al. “A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population.” Nutrients 16(1) (2023)
Allele G
OR 0.06
p 4.0e-8
N 107,230
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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