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Variantes que influyen en Preeclampsia 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
1421085
Genotype
C
C
Level of evidence
Probabilidad aumentada
Unisex
2 Sources
Participants: 760882
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
2 Sources
Participants: 760882
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
2 Sources
Participants: 760882
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
2 Sources
Participants: 760882
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.
10774624
Genotype
A
A
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters G/G is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters C/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
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
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
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters G/G is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters C/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
G
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
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.
1458038
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters T/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
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
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
T
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
The genotype with the letters T/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
T
Level of evidence
Probabilidad aumentada
Unisex
1 Sources
Participants: 167234
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.