Condición
Duodenal ulcer
Desafortunadamente, aún no tenemos más datos para esta página. Más contenido próximamente.
Variantes que influyen en Duodenal ulcer 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
2294008
Genotype
C
C
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 22737
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
T
T
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 22737
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: 22737
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
T
T
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 22737
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.
8126001
Genotype
T
T
Level of evidence
Probabilidad reducida
Unisex
1 Sources
Participants: 884325
The genotype with the letters T/T is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.
Genotype
C
T
Level of evidence
Probabilidad reducida
Unisex
1 Sources
Participants: 884325
The genotype with the letters C/T is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad reducida
Unisex
1 Sources
Participants: 884325
The genotype with the letters T/T is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.
Genotype
C
T
Level of evidence
Probabilidad reducida
Unisex
1 Sources
Participants: 884325
The genotype with the letters C/T is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.