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Variants that influence Schizophrenia 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 Concern Both Biological Males and Females

Genotype

G

G

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

G

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

T

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

G

G

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

G

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

T

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

C

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

C

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

T

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

C

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

C

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

T

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

No available data

Genotype

T

T

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

The genotype with the letters T/T 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

C

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters C/T 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

C

C

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters C/C 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

T

T

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 0

The genotype with the letters T/T 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

C

T

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters C/T 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

C

C

Level of evidence

doctor_quote

Unknown effect

Unisex

1 Sources

Participants: 0

The genotype with the letters C/C 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.

Variants that influence Schizophrenia based on Scientific Studies

Scientific studies classifications aim to uncover how genetic variants function and their roles in diseases, traits, and evolution. Variants are categorized based on their functional impact, such as loss-of-function (reduces gene activity), gain-of-function (increases gene activity), neutral (no significant impact), or evolutionary conservation. This classification uses experimental data, population studies, and computational analyses to understand variant effects. Unlike clinical testing, which focuses on immediate health impacts, scientific studies explore broader genetic mechanisms and long-term implications.

Variants that Concern Both Biological Males and Females

Genotype

A

A

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

C

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

The genotype with the letters A/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

C

Level of evidence

doctor_quote

No Effect

Unisex

0 Sources

Participants: 0

No available data

Genotype

A

A

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

C

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

The genotype with the letters A/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

C

Level of evidence

doctor_quote

No Effect

Unisex

0 Sources

Participants: 0

No available data

Genotype

A

A

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

doctor_quote

No Effect

Unisex

0 Sources

Participants: 0

No available data

Genotype

A

A

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 466574

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

doctor_quote

No Effect

Unisex

0 Sources

Participants: 0

No available data

Genotype

C

C

Level of evidence

doctor_quote

Increased likelihood

Unisex

4 Sources

Participants: 465676

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

T

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 542772

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

T

T

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 77096

No available data

Genotype

C

C

Level of evidence

doctor_quote

Increased likelihood

Unisex

4 Sources

Participants: 465676

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

T

Level of evidence

doctor_quote

Increased likelihood

Unisex

5 Sources

Participants: 542772

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

T

T

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 77096

No available data

Variants that influence Schizophrenia

Genes that influence Schizophrenia

Drugs influenced by genetics

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