Gene: NLRP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55655
Gene Symbol: NLRP2
NLRP2 		0.010 GeneticVariation disease BEFREE A truncating deletion [657del(5)] in exon 6 of the nibrin NBS1 gene is the most frequent cause of the syndrome. 12505263 2002