rs4925659, NLRP3

N. diseases: 3
Disease: Fibrinogen, CTCAE ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265 2011