CondiciĂłn
Autoimmune lymphoproliferative syndrome
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Variantes que influyen en Autoimmune lymphoproliferative syndrome segĂşn las pruebas clĂnicas
Las clasificaciones de pruebas clĂnicas están diseñadas para ayudar a los mĂ©dicos a comprender cĂłmo los cambios genĂ©ticos, conocidos como variantes, podrĂan afectar la salud de una persona y guiar las decisiones mĂ©dicas. 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 clasificaciĂłn se basa en una combinaciĂłn 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 biolĂłgicas
121913080
Genotype
A
A
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
G
G
Level of evidence
Sin efecto
Unisex
2 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
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G 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
C
G
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
A
A
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
G
G
Level of evidence
Sin efecto
Unisex
2 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
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G 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
C
G
Level of evidence
Causante de enfermedad
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G is considered disease causing. Carriers of this genetic result are typically affected by the disease.
267607122
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.