Condición
Generalized epilepsy-paroxysmal dyskinesia syndrome
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Variantes que influyen en Generalized epilepsy-paroxysmal dyskinesia syndrome según las pruebas clínicas
Las clasificaciones de pruebas clínicas están diseñadas para ayudar a los médicos a comprender cómo los cambios genéticos, conocidos como variantes, podrían afectar la salud de una persona y guiar las decisiones médicas. Las variantes se etiquetan como Causantes de Enfermedad (dañinas), Probablemente Causantes de Enfermedad, Efecto Desconocido (impacto desconocido), Probablemente Sin Efecto (probablemente no dañinas) y Sin Efecto (no dañinas). Esta clasificación se basa en una combinación de antecedentes familiares, pruebas de laboratorio y predicciones por computadora para determinar el impacto de las variantes.
Variantes que afectan tanto a hombres como a mujeres biológicas
45527834
Genotype
A
A
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
G
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
A
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
G
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
137853333
Genotype
C
C
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
C
C
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.
863224885
Genotype
C
C
Level of evidence
Probablemente causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Probablemente causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
C
C
Level of evidence
Probablemente causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Probablemente causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.