Zustand
Atrial fibrillation
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Varianten, die Atrial fibrillation basierend auf klinischen Tests beeinflussen
Klinische Testklassifikationen sind darauf ausgelegt, Ärzten dabei zu helfen, zu verstehen, wie genetische Veränderungen, bekannt als Varianten, die Gesundheit einer Person beeinflussen könnten und medizinische Entscheidungen leiten. Varianten werden als Krankheitsverursachend (schädlich), Wahrscheinlich Krankheitsverursachend, Unbekannte Wirkung (unbekannte Auswirkung), Wahrscheinlich Keine Wirkung (wahrscheinlich nicht schädlich) und Keine Wirkung (nicht schädlich) gekennzeichnet. Diese Klassifizierung stützt sich auf eine Mischung aus Familiengeschichte, Labortests und Computerprognosen, um die Auswirkungen der Varianten zu bestimmen.
Varianten, die sowohl biologische Männer als auch Frauen betreffen
Genotype
C
C
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G has 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
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G has 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
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
A
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
A
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
No available data
Varianten, die Atrial fibrillation basierend auf wissenschaftlichen Studien beeinflussen
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.
Varianten, die sowohl biologische Männer als auch Frauen betreffen
Genotype
C
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
5 Sources
Participants: 1300352
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
5 Sources
Participants: 1300352
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
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
5 Sources
Participants: 1300352
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
5 Sources
Participants: 1300352
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
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
6 Sources
Participants: 5158915
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
6 Sources
Participants: 5158915
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
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
6 Sources
Participants: 5158915
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
6 Sources
Participants: 5158915
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
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
5 Sources
Participants: 5122123
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
5 Sources
Participants: 5122123
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
C
Level of evidence
Kein Effekt
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Erhöhte Wahrscheinlichkeit
Unisex
5 Sources
Participants: 5122123
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
5 Sources
Participants: 5122123
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.