RIT1, Ras like without CAAX 1, 6016

N. diseases: 184; N. variants: 18
Disease: Abnormality of refraction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025195
rs869025195
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4025843
Disease:
Abnormality of refraction 		G 0.700 CausalMutation CLINVAR