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Variants that influence Familial nephrotic syndrome 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

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

T

T

Level of evidence

Unknown effect

Unisex

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

Unknown effect

Unisex

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

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

T

T

Level of evidence

Unknown effect

Unisex

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

Unknown effect

Unisex

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

Unknown effect

Unisex

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

T

T

Level of evidence

No Effect

Unisex

1 Sources

Participants: 0

The genotype with the letters T/T 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

T

Level of evidence

Unknown effect

Unisex

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

Unknown effect

Unisex

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

T

T

Level of evidence

No Effect

Unisex

1 Sources

Participants: 0

The genotype with the letters T/T 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

T

Level of evidence

Unknown effect

Unisex

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.

77309273

Genotype

A

A

Level of evidence

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters A/A 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

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

A

C

Level of evidence

Unknown effect

Unisex

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

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters A/A 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

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

A

C

Level of evidence

Unknown effect

Unisex

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.

Variants that influence Familial nephrotic syndrome

Genes that influence Familial nephrotic syndrome

Drugs influenced by genetics

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