Condición
Moyamoya disease
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Variantes que influyen en Moyamoya disease 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
5030766
Genotype
A
A
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A 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
G
G
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters G/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
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
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A 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
G
G
Level of evidence
Probablemente sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters G/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
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.
Variantes que influyen en Moyamoya disease según estudios científicos
Las clasificaciones de estudios científicos tienen como objetivo descubrir cómo funcionan las variantes genéticas y su papel en las enfermedades, los rasgos y la evolución. Las variantes se categorizan según su impacto funcional, como pérdida de función (reduce la actividad génica), ganancia de función (aumenta la actividad génica), neutral (sin impacto significativo) o conservación evolutiva. Esta clasificación utiliza datos experimentales, estudios de población y análisis computacionales para comprender los efectos de las variantes. A diferencia de las pruebas clínicas, que se centran en los impactos inmediatos en la salud, los estudios científicos exploran mecanismos genéticos más amplios e implicaciones a largo plazo.
Variantes que afectan tanto a hombres como a mujeres biológicas
2107595
Genotype
A
A
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/A is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/G is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
A
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/A is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/G is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
2273291
Genotype
A
A
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/A is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
A
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/A is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
A
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 2786
The genotype with the letters A/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
3853818
Genotype
C
C
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 512
The genotype with the letters C/C is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 512
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 512
The genotype with the letters C/C is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 512
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.