rs28941785

This is a variant in the CTH gene that changes a threonine to an isoleucine.

GWAS Catalog Trait Associations (2)

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

cystathionine measurement

Allele T
OR 1.44
p 5.0e-147
N 14,296
Large GWAS
European
Allele T
OR 0.92
p 7.0e-34
N 8,014
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 1.23
p 1.0e-45
N 6,075
Large GWAS
multi-ancestry

X-11795 measurement

Allele T
OR 1.00
p 7.0e-74
N 14,296
Large GWAS
European
Allele T
OR 0.88
p 1.0e-32
N 8,809
Large GWAS
European
Allele T
OR 0.79
p 1.0e-26
N 8,238
Large GWAS
European

ClinVar annotation

Pathogenic★★★
8 submitters6 publications

CTH-related disorder; Cystathioninuria

View on ClinVar →

About CTH

This gene encodes a cytoplasmic enzyme in the trans-sulfuration pathway that converts cystathione derived from methionine into cysteine. Glutathione synthesis in the liver is dependent upon the availability of cysteine. Mutations in this gene cause cystathioninuria. Alternative splicing of this gene results in three transcript variants encoding different isoforms. [provided by RefSeq, Jun 2010]

View all CTH variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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