Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4893
Gene Symbol: NRAS
NRAS 		0.700 CausalMutation disease CLINVAR
Entrez Id: 3845
Gene Symbol: KRAS
KRAS 		0.630 CausalMutation disease CLINVAR Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutations. 24803665 2014
Entrez Id: 3845
Gene Symbol: KRAS
KRAS 		0.630 CausalMutation disease CLINVAR Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders. 20949621 2011
Entrez Id: 3845
Gene Symbol: KRAS
KRAS 		0.630 CausalMutation disease CLINVAR Germline KRAS mutations cause Noonan syndrome. 16474405 2006
Entrez Id: 3845
Gene Symbol: KRAS
KRAS 		0.630 GeneticVariation disease CLINVAR
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR Autoimmune pancreatitis in the autoimmune lymphoproliferative syndrome (ALPS): a sheep in wolves' clothing? 23407489 2013
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance. 22237435 2012
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome. 21490157 2011
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 GeneticVariation disease CLINVAR FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome. 21490157 2011
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR Inherited perforin and Fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphoma. 15459303 2004
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR Fas preassociation required for apoptosis signaling and dominant inhibition by pathogenic mutations. 10875918 2000
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 CausalMutation disease CLINVAR Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance. 10090885 1999
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 GeneticVariation disease CLINVAR Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance. 10090885 1999
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.110 GeneticVariation disease CLINVAR The molecular basis for apoptotic defects in patients with CD95 (Fas/Apo-1) mutations. 9927496 1999
Entrez Id: 356
Gene Symbol: FASLG
FASLG 		0.100 CausalMutation disease CLINVAR
Entrez Id: 843
Gene Symbol: CASP10
CASP10 		0.100 CausalMutation disease CLINVAR