rs878853161, SLC2A1

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seizures
CUI: C0036572
Disease: Seizures
0.700 CausalMutation CLINVAR
Moderate intellectual disability
CUI: C0026351
Disease: Moderate intellectual disability
0.700 CausalMutation CLINVAR
Congenital anomaly of face
CUI: C0266617
Disease: Congenital anomaly of face
0.700 CausalMutation CLINVAR
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.700 CausalMutation CLINVAR
GLUT1 DEFICIENCY SYNDROME 1
CUI: C4551966
Disease: GLUT1 DEFICIENCY SYNDROME 1
0.700 CausalMutation CLINVAR
Dystonia
CUI: C0013421
Disease: Dystonia
0.700 CausalMutation CLINVAR
Speech Delay
CUI: C0241210
Disease: Speech Delay
0.700 CausalMutation CLINVAR