TNXB, tenascin XB, 7148

N. diseases: 127; N. variants: 79
Disease: C4 complement assay (procedure) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.100 GeneticVariation phenotype GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269 2017
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341 2012
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341 2012