rs6088813

This variant is located in the UQCC1 gene.

GWAS Catalog Trait Associations (2)

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

body height

Allele C
OR 0.07
p 1.0e-38
N 67,452
Large GWAS
East Asian

vital capacity

Allele C
OR 8.91
p 5.0e-19
N 68,470
Meta-analysisLarge GWAS
multi-ancestry

Research that mentions this SNP (1)

A genome‐wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22
AssociationN=53,938Hanneke J. M. Kerkhof et al.(2010)· Arthritis &amp; Rheumatism

Genome-wide association study identifying 14,938 osteoarthritis cases and approximately 39,000 controls found that the C-allele of rs3815148 on chromosome 7q22 (near GPR22 gene) is associated with 1.14-fold increased risk of knee/hand OA (p=8×10⁻⁸) and 30% increased risk for knee OA progression. The same study identified rs10248619 and rs6088813 with secondary associations to OA.

Traits studied:Hand osteoarthritisHip osteoarthritisKnee osteoarthritisKnee osteoarthritis progressionOsteoarthritis

About UQCC1

This gene encodes a transmembrane protein that is structurally similar to the mouse basic fibroblast growth factor repressed ZIC-binding protein. In mouse this protein may be involved in fibroblast growth factor regulated growth control. In humans, polymorphisms in this gene are associated with variation in human height and osteoarthritis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

View all UQCC1 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…