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 		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
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