CLGN, calmegin, 1047

N. diseases: 11; N. variants: 4
Disease: Mean blood pressure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2567241
rs2567241
Entrez Id: 1047
Gene Symbol: CLGN
CLGN
CUI: C0428886
Disease:
Mean blood pressure 		0.700 GeneticVariation GWASCAT Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. 27271309 2016