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Variantes que influyen en Idiopathic inflammatory myopathy 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

Genotype

A

A

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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: 18207

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

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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: 18207

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: 18207

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

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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.

10189330

Genotype

T

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

G

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

The genotype with the letters G/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

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

T

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

G

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

The genotype with the letters G/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

T

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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.

3129843

Genotype

G

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

A

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

G

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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

A

G

Level of evidence

Probabilidad aumentada

Unisex

1 Sources

Participants: 18207

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.

Variantes que influyen en Idiopathic inflammatory myopathy

Genes que influyen en Idiopathic inflammatory myopathy

Medicamentos influenciados por la genética

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