MSH5, mutS homolog 5, 4439

N. diseases: 51; N. variants: 23
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