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Variants that influence Esophageal varix 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 Affect Both Biological Males and Females
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
A
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
A
A
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
A
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
A
A
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
G
Level of evidence
No Effect
Unisex
1 Sources
Participants: 613934
No available data
Genotype
G
G
Level of evidence
Reduced likelihood
Unisex
1 Sources
Participants: 613934
The genotype with the letters G/G is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
G
Level of evidence
No Effect
Unisex
1 Sources
Participants: 613934
No available data
Genotype
G
G
Level of evidence
Reduced likelihood
Unisex
1 Sources
Participants: 613934
The genotype with the letters G/G is considered protective. Carriers of this genetic result are at reduced risk of developing the disease.
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
C
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data
Genotype
T
T
Level of evidence
No Effect
Unisex
0 Sources
Participants: 0
No available data