rs6060373, UQCC1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008
Congenital Dysplasia Of The Hip
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
0.010 GeneticVariation BEFREE Our study demonstrates common variants of UQCC, specifically rs6060373, are associated with DDH in Han Chinese population. 25848760 2015
Testicular Germ Cell Tumor
CUI: C1336708
Disease: Testicular Germ Cell Tumor
0.010 GeneticVariation BEFREE Two SNPs were found to be associated with risk of TGCT, rs6060373 (CC vs TT, OR = 1.51, 95% CI: 1.06-2.15) and rs143384 (CC vs TT, OR = 1.53, 95% CI: 1.09-2.15). rs6060373 is an intronic polymorphism of ubiquinol-cytochrome c reductase complex chaperone (UQCC), and rs143384 is a 5'UTR polymorphism of growth differentiation factor 5 (GDF5). 21233139 2011