rs17410962

This is a intergenic variant variant.

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GWAS Catalog Trait Associations (8)

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

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 0.20
p 2.0e-28
N 107,230
Large GWAS
East Asian

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 A
OR 8.33
p 5.0e-28
N 33,431
Large GWAS
European
Coram MA et al. “Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.” American Journal of Human Genetics 92(6):904-16 (2013)
Allele A
OR 0.11
p 7.0e-9
N 10,936
Large GWAS
multi-ancestry

fatty acid amount

Sun Y et al. “GWAS and multi-omics integrative analysis reveal novel loci and their molecular mechanisms for circulating fatty acids.” Hgg Advances 6(4):100470 (2025)
Allele A
OR —
p 9.0e-21
N 128,922
Large GWAS
European

type 2 diabetes mellitus

Elashi AA et al. “Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus.” Bmc Medical Genomics 17(1):115 (2024)
Allele A
OR 0.05
p 1.0e-11
N 6,710,881
Meta-analysisLarge GWAS
multi-ancestry

familial hyperlipidemia

Trinder M et al. “Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia.” Atherosclerosis 340:35-43 (2022)
Allele G
OR 0.39
p 3.0e-23
N 349,222
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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