rs267606920, NRAS

N. diseases: 4
Disease: Noonan Syndrome 6 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Noonan Syndrome 6
CUI: C2750732
Disease: Noonan Syndrome 6
0.800 GeneticVariation UNIPROT A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
Noonan Syndrome 6
CUI: C2750732
Disease: Noonan Syndrome 6
0.800 GeneticVariation UNIPROT Noonan syndrome: clinical features, diagnosis, and management guidelines. 20876176 2010
Noonan Syndrome 6
CUI: C2750732
Disease: Noonan Syndrome 6
0.800 CausalMutation CLINVAR