Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9949
Gene Symbol: AMMECR1
AMMECR1 		0.400 CausalMutation phenotype CLINVAR
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11 		0.100 CausalMutation phenotype CLINVAR The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. 15928039 2005
Entrez Id: 9862
Gene Symbol: MED24
MED24 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 8532
Gene Symbol: CPZ
CPZ 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 57504
Gene Symbol: MTA3
MTA3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 220001
Gene Symbol: VWCE
VWCE 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 5894
Gene Symbol: RAF1
RAF1 		0.100 CausalMutation phenotype CLINVAR Germline gain-of-function mutations in RAF1 cause Noonan syndrome. 17603482 2007
Entrez Id: 1294
Gene Symbol: COL7A1
COL7A1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6261
Gene Symbol: RYR1
RYR1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 8467
Gene Symbol: SMARCA5
SMARCA5 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 154881
Gene Symbol: KCTD7
KCTD7 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 2778
Gene Symbol: GNAS
GNAS 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6249
Gene Symbol: CLIP1
CLIP1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 4882
Gene Symbol: NPR2
NPR2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 5888
Gene Symbol: RAD51
RAD51 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 23476
Gene Symbol: BRD4
BRD4 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 3899
Gene Symbol: AFF3
AFF3 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 51119
Gene Symbol: SBDS
SBDS 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 118429
Gene Symbol: ANTXR2
ANTXR2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 64319
Gene Symbol: FBRS
FBRS 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 50485
Gene Symbol: SMARCAL1
SMARCAL1 		0.100 CausalMutation phenotype CLINVAR