RIT1, Ras like without CAAX 1, 6016

N. diseases: 184; N. variants: 18
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: rs1557960039
rs1557960039
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C3809233
Disease:
NOONAN SYNDROME 8 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1557962794
rs1557962794
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0018817
Disease:
Atrial Septal Defects 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1557962794
rs1557962794
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4551602
Disease:
Noonan Syndrome 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1557962794
rs1557962794
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1956257
Disease:
Pulmonary Stenosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0008733
Disease:
Chylothorax 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4025753
Disease:
Abnormal tricuspid valve morphology 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1844806
Disease:
Weight less than 3rd percentile 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C3164445
Disease:
Abnormality of aortic valve 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0032227
Disease:
Pleural effusion disorder 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0424503
Disease:
Dysmorphic facies 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0018818
Disease:
Ventricular Septal Defects 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0020224
Disease:
Polyhydramnios 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0031039
Disease:
Pericardial effusion 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0151526
Disease:
Premature Birth 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C3809233
Disease:
NOONAN SYNDROME 8 		A 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4025759
Disease:
Abnormal mitral valve morphology 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1836940
Disease:
Thickened nuchal skin fold 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0020305
Disease:
Hydrops Fetalis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs483352822
rs483352822
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0005779
Disease:
Blood Coagulation Disorders 		G 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1285291
Disease:
Fetal ascites 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0032227
Disease:
Pleural effusion disorder 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0151526
Disease:
Premature Birth 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0008733
Disease:
Chylothorax 		C 0.700 CausalMutation CLINVAR