rs1060500046
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs1060500046
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770624
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770667
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
T |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs797045047
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs797045047
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs869312865
|
GRIN1;LOC105376328
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
|
C |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554770064
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
GAGC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770185
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
CCGGCAT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770262
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770589
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554770667
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564363665
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564365418
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Large head (disorder)
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564365418
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Febrile Convulsions
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564365418
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Autistic behavior
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564365418
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Expressive language delay
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1564365418
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Global developmental delay
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs200777850
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs781053477
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs797044925
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs869312865
|
GRIN1;LOC105376328
|
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs869312865
|
GRIN1;LOC105376328
|
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs878853143
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Mental Retardation
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554770044
|
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus.
|
6306230 |
1983 |