rs3935209

This variant is located in the OPLAH gene.

GWAS Catalog Trait Associations (5)

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

5-oxoproline measurement

Allele G
OR 0.82
p 3.0e-220
N 8,247
Large GWAS
European
Allele G
OR 0.34
p 9.0e-76
N 14,296
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 G
OR 0.51
p 3.0e-122
N 9,369
Large GWAS
multi-ancestry
Allele G
OR 0.22
p 2.0e-83
N 4,960
Large GWAS
European

6-oxopiperidine-2-carboxylate measurement

Allele T
OR 0.48
p 6.0e-150
N 14,296
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 0.54
p 2.0e-102
N 7,856
Large GWAS
multi-ancestry
Allele T
OR 0.64
p 2.0e-68
N 6,136
Large GWAS
European
Allele T
OR 0.22
p 8.0e-26
N 4,540
Large GWAS
European

serum metabolite level

Allele T
OR 0.72
p 4.0e-100
N 3,926
Large GWAS
Hispanic or Latin American

ClinVar annotation

Benign★★★
3 submitters2 publications

5-Oxoprolinase deficiency; OPLAH-related disorder; not provided

View on ClinVar →

About OPLAH

The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]

View all OPLAH 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…