Gene: NLRP3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3 		0.400 GeneticVariation disease CLINVAR Keratoendotheliitis fugax hereditaria is an autoinflammatory cryopyrin-associated periodic syndrome caused by a missense mutation c.61G>C in exon 1 of NLRP3 in Finnish patients. 29366613 2018
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3 		0.400 GeneticVariation disease UNIPROT Keratoendotheliitis fugax hereditaria is an autoinflammatory cryopyrin-associated periodic syndrome caused by a missense mutation c.61G>C in exon 1 of NLRP3 in Finnish patients. 29366613 2018
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3 		0.400 CausalMutation disease CLINVAR