Condition
Dilated cardiomyopathy 1HH
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Variants qui influencent Dilated cardiomyopathy 1HH 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
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
C
C
Level of evidence
Sans effet
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/C is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
C
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters C/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.
Genotype
T
T
Level of evidence
Effet inconnu
Unisexe
1 Sources
Participants: 0
The genotype with the letters T/T is considered disease causing. Carriers of this genetic result are typically affected by the disease.