Condition
Benign concentric annular macular dystrophy
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Variants that influence Benign concentric annular macular dystrophy based on Clinical Testing
Clinical testing classifications are designed to help doctors understand how genetic changes, known as variants, might affect a person’s health and guide medical decisions. Variants are labeled as Disease Causing (harmful), likely Disease Causing, Unknown Effect (unknown impact), Likely No Effect (likely not harmful), and No Effect (not harmful). This classification relies on a mix of family history, lab tests, and computer predictions to determine the impact of variants.
Variants that Affect Both Biological Males and Females
Genotype
A
A
Level of evidence
No Effect
Unisex
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
A
G
Level of evidence
Likely disease causing
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
G
G
Level of evidence
Likely disease causing
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
A
A
Level of evidence
No Effect
Unisex
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
A
G
Level of evidence
Likely disease causing
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
G
G
Level of evidence
Likely disease causing
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is considered likely disease causing. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are often affected by the disease.
Genotype
G
G
Level of evidence
No Effect
Unisex
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
No Effect
Unisex
1 Sources
Participants: 0
The genotype with the letters C/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
C
Level of evidence
No Effect
Unisex
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
G
G
Level of evidence
No Effect
Unisex
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
No Effect
Unisex
1 Sources
Participants: 0
The genotype with the letters C/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
C
Level of evidence
No Effect
Unisex
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.