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Variants qui influencent Myelofibrosis 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
77375493
Genotype
G
G
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/G 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
G
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
G
G
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/G 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
G
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
202080221
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
G
G
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/G 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
G
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/G 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
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
G
G
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters G/G 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
G
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.