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: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1956257
Disease:
Pulmonary Stenosis 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0005745
Disease:
Blepharoptosis 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4021797
Disease:
Abnormality of the thorax 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0349588
Disease:
Short stature 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C2674608
Disease:
Feeding difficulties in infancy 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1854301
Disease:
Motor delay 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1843367
Disease:
Poor school performance 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0020224
Disease:
Polyhydramnios 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0521525
Disease:
Short neck 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601334
rs672601334
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4551602
Disease:
Noonan Syndrome 1 		C 0.700 CausalMutation CLINVAR
dbSNP: rs672601335
rs672601335
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4551602
Disease:
Noonan Syndrome 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0005745
Disease:
Blepharoptosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4023676
Disease:
Increased nuchal translucency 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0521525
Disease:
Short neck 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0020305
Disease:
Hydrops Fetalis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0240278
Disease:
Lymphatic obstruction 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4025843
Disease:
Abnormality of refraction 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0349588
Disease:
Short stature 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4551602
Disease:
Noonan Syndrome 1 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C1854301
Disease:
Motor delay 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C2674608
Disease:
Feeding difficulties in infancy 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C4025759
Disease:
Abnormal mitral valve morphology 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730881014
rs730881014
Entrez Id: 6016
Gene Symbol: RIT1
RIT1
CUI: C0028326
Disease:
Noonan Syndrome 		C 0.700 CausalMutation CLINVAR