rs68149176

This is a regulatory region variant variant in the SLC7A5 gene.

GWAS Catalog Trait Associations (5)

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

mean reticulocyte volume

Allele T
OR 0.04
p 2.0e-67
N 394,642
Large GWAS
European

erythrocyte volume

Allele T
OR 0.04
p 3.0e-65
N 544,127
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.04
p 4.0e-60
N 408,112
Large GWAS
European
Allele T
OR 0.03
p 7.0e-50
N 394,642
Large GWAS
European
Allele T
OR 0.04
p 4.0e-20
N 172,433
Large GWAS
European

mean corpuscular hemoglobin

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.04
p 9.0e-52
N 408,112
Large GWAS
European
Allele T
OR 0.03
p 5.0e-49
N 394,642
Large GWAS
European
Allele T
OR 0.03
p 8.0e-17
N 172,332
Large GWAS
European

mean corpuscular hemoglobin concentration

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 C
OR 0.03
p 4.0e-19
N 583,889
Major Consortium StudyLarge GWAS
multi-ancestry

pyruvate measurement

Allele C
OR 0.03
p 1.0e-8
N 114,749
Large GWAS
European

About SLC7A5

Enables L-amino acid transmembrane transporter activity and secondary active transmembrane transporter activity. Involved in carboxylic acid transport; thyroid hormone transport; and xenobiotic transport. Located in several cellular components, including apical plasma membrane; cytosol; and microvillus membrane. Part of amino acid transport complex. Implicated in cholangiocarcinoma; colon cancer; hepatocellular carcinoma; and lung squamous cell carcinoma. Biomarker of esophagitis; gastrointestinal system cancer (multiple); malignant astrocytoma (multiple); and respiratory system cancer (multiple). [provided by Alliance of Genome Resources, Apr 2025]

View all SLC7A5 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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