Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6237
Gene Symbol: RRAS
RRAS
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.510 Biomarker CLINGEN We report on two germline mutations (p.Gly39dup and p.Val55Met) in RRAS, a gene encoding a small monomeric GTPase controlling cell adhesion, spreading and migration, underlying a rare (2 subjects among 504 individuals analysed) and variable phenotype with features partially overlapping Noonan syndrome, the most common RASopathy. 24705357

2014
Entrez Id: 6237
Gene Symbol: RRAS
RRAS
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.510 Biomarker CLINGEN The RASopathies. 23875798

2013