rs188247550

This is a intron variant variant in the SUGP1 gene.

GWAS Catalog Trait Associations (30)

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

triglyceride measurement

Allele C
OR 0.12
p 4.0e-45
N 394,642
Large GWAS
European
Koskeridis F et al. Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Nature Communications 13(1):6939 (2022)
Allele C
OR 0.12
p 6.0e-30
N 361,194
Large GWAS
European

total cholesterol measurement

Allele T
OR 0.13
p 2.0e-46
N 394,642
Large GWAS
European

low density lipoprotein cholesterol measurement

Allele T
OR 0.12
p 2.0e-39
N 394,642
Large GWAS
European
Koskeridis F et al. Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Nature Communications 13(1):6939 (2022)
Allele T
OR 0.07
p 4.0e-28
N 361,194
Large GWAS
European

alkaline phosphatase measurement

Allele T
OR 0.09
p 2.0e-31
N 394,642
Large GWAS
European

cathepsin O measurement

Allele T
OR 0.26
p 2.0e-29
N 47,745
Large GWAS
European

non-alcoholic fatty liver disease

Allele C
OR 0.33
p 1.0e-23
N 122,644
Large GWAS
European

protein CREG1 measurement

Allele T
OR 0.22
p 8.0e-23
N 47,745
Large GWAS
European

About SUGP1

SF4 is a member of the SURP family of splicing factors.[supplied by OMIM, Sep 2003]

View all SUGP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…