Gene: NLRP7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 199713
Gene Symbol: NLRP7
NLRP7 		0.500 GeneticVariation disease BEFREE A familial or sporadic recurrent hydatidiform mole is a rare autosomal recessive condition that has been associated with biallelic mutations in the nucleotide-binding, leucine-rich repeat, pyrin domain 7 (NLRP7) gene (19q13.42). 21623199 2011
Entrez Id: 199713
Gene Symbol: NLRP7
NLRP7 		0.500 CausalMutation disease CLINVAR Homozygous NLRP7 mutations in a Moroccan woman with recurrent reproductive failure. 19054016 2009
Entrez Id: 199713
Gene Symbol: NLRP7
NLRP7 		0.500 CausalMutation disease CLINVAR A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles. 18039680 2008