Wissenschaftliche Studienklassifikationen zielen darauf ab, herauszufinden, wie genetische Varianten funktionieren und welche Rolle sie bei Krankheiten, Merkmalen und der Evolution spielen. Varianten werden basierend auf ihrer funktionellen Auswirkung kategorisiert, wie etwa Funktionsverlust (verringert die Genaktivität), Funktionsgewinn (erhöht die Genaktivität), neutral (keine signifikante Auswirkung) oder evolutionäre Konservierung. Diese Klassifizierung nutzt experimentelle Daten, Populationsstudien und computerbasierte Analysen, um die Auswirkungen von Varianten zu verstehen. Im Gegensatz zu klinischen Tests, die sich auf unmittelbare gesundheitliche Auswirkungen konzentrieren, erforschen wissenschaftliche Studien breitere genetische Mechanismen und langfristige Implikationen.
Genotype
T
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
G
G
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
G
G
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
G
G
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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
Erhöhte Wahrscheinlichkeit
Unisex
1 Sources
Participants: 5161
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.