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Variants qui influencent Kidney disease selon les tests cliniques
Les classifications des tests cliniques sont conçues pour aider les médecins à comprendre comment les changements génétiques, appelés variants, pourraient affecter la santé d'une personne et orienter les décisions médicales. Les variants sont étiquetés comme Causant une Maladie (nocifs), Probablement Causant une Maladie, Effet Inconnu (impact inconnu), Probablement Sans Effet (probablement non nocifs) et Sans Effet (non nocifs). Cette classification repose sur un mélange d'antécédents familiaux, de tests de laboratoire et de prédictions informatiques pour déterminer l'impact des variants.
Variantes concernant à la fois les hommes et les femmes biologiques
5707
Genotype
A
A
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
C
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters A/C has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
A
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
C
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters A/C has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
203687
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
11571117
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have 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
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Variants qui influencent Kidney disease selon des études scientifiques
Les classifications des études scientifiques visent à découvrir comment les variantes génétiques fonctionnent et leur rôle dans les maladies, les traits et l'évolution. Les variantes sont catégorisées en fonction de leur impact fonctionnel, comme la perte de fonction (réduit l'activité du gène), le gain de fonction (augmente l'activité du gène), neutre (pas d'impact significatif) ou la conservation évolutive. Cette classification utilise des données expérimentales, des études de population et des analyses informatiques pour comprendre les effets des variantes. Contrairement aux tests cliniques, qui se concentrent sur les impacts immédiats sur la santé, les études scientifiques explorent des mécanismes génétiques plus larges et des implications à long terme.
Variantes concernant à la fois les hommes et les femmes biologiques
55703767
Genotype
G
G
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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
T
T
Level of evidence
Sans effet
Unisexe
0 Sources
Participants: 0
No available data
Genotype
G
T
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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
G
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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
T
T
Level of evidence
Sans effet
Unisexe
0 Sources
Participants: 0
No available data
Genotype
G
T
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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
G
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 14753
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.
72831309
Genotype
A
A
Level of evidence
Probabilité accrue
Unisexe
2 Sources
Participants: 22444
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
G
Level of evidence
Probabilité accrue
Unisexe
2 Sources
Participants: 22444
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
Probabilité accrue
Unisexe
2 Sources
Participants: 22444
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
G
Level of evidence
Probabilité accrue
Unisexe
2 Sources
Participants: 22444
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.
7562121
Genotype
C
C
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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
G
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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
C
T
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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
G
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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
C
T
Level of evidence
Probabilité accrue
Unisexe
1 Sources
Participants: 4808
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.