rs17843929

This is a intron variant variant in the PPID gene.

GWAS Catalog Trait Associations (6)

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

peptidyl-prolyl cis-trans isomerase D measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele T
OR 0.49
p 2.0e-276
N 10,708
Large GWAS
European

octanoylcarnitine measurement

Allele T
OR 0.28
p 7.0e-37
N 6,136
Large GWAS
European
Allele T
OR 0.19
p 1.0e-29
N 8,226
Large GWAS
European

decanoylcarnitine measurement

Allele T
OR 0.28
p 5.0e-35
N 6,136
Large GWAS
European

nonanoylcarnitine (C9) measurement

Allele T
OR 0.26
p 4.0e-28
N 6,136
Large GWAS
European

laurylcarnitine measurement

Allele T
OR 0.20
p 1.0e-18
N 6,136
Large GWAS
European
Feofanova EV et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications 14(1):3111 (2023)
Allele T
OR 0.15
p 2.0e-18
N 10,341
Large GWAS
multi-ancestry

carnitine measurement

Allele C
OR 8.66
p 5.0e-18
N 9,363
Large GWAS
European

About PPID

The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein has been shown to possess PPIase activity and, similar to other family members, can bind to the immunosuppressant cyclosporin A. [provided by RefSeq, Jul 2008]

View all PPID 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…