RIT1, Ras like without CAAX 1, 6016

N. diseases: 184; N. variants: 18
Disease: Noonan Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025194
rs869025194
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0028326
Disease:
Noonan Syndrome 		G 0.710 CausalMutation CLINVAR
dbSNP: rs869025194
rs869025194
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0028326
Disease:
Noonan Syndrome 		C 0.710 CausalMutation CLINVAR
dbSNP: rs869025194
rs869025194
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0028326
Disease:
Noonan Syndrome 		0.710 GeneticVariation BEFREE All five mutations are associated with NS, whereas two (A57G and F82V) have also been identified in urinary tract cancers and myeloid malignancies. 27226556 2016