rs35372182

This is a intergenic variant variant in the SYNE2 gene.

GWAS Catalog Trait Associations (10)

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

Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement

Allele A
OR 0.45
p 7.0e-239
N 14,296
Large GWAS
European

Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement

Allele A
OR 0.27
p 8.0e-88
N 14,296
Large GWAS
European

sphingomyelin measurement

Allele G
OR 0.15
p 2.0e-48
N 4,959
Large GWAS
European
Allele G
OR 0.07
p 2.0e-12
N 5,662
Large GWAS
South Asian

stearoyl sphingomyelin (d18:1/18:0) measurement

Allele A
OR 0.11
p 1.0e-14
N 14,296
Large GWAS
European

triglyceride measurement

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 A
OR 0.03
p 3.0e-13
N 391,247
Major Consortium StudyLarge GWAS
European

serum metabolite level

Allele A
OR 0.18
p 2.0e-11
N 3,926
Large GWAS
Hispanic or Latin American

level of ceramide

Allele A
OR 0.19
p 2.0e-9
N 1,954
Large GWAS
East Asian

About SYNE2

The protein encoded by this gene is a nuclear outer membrane protein that binds cytoplasmic F-actin. This binding tethers the nucleus to the cytoskeleton and aids in the maintenance of the structural integrity of the nucleus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

View all SYNE2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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