| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +6 more | |
| | | Single nucleotide variant (synonymous variant) | C3-related disorder +4 more | |
| | | Single nucleotide variant (missense variant) | C3-related disorder +4 more | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (intron variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Age related macular degeneration 9 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | C3-related disorder +4 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +5 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (intron variant) | C3-related disorder +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (intron variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +4 more | |
| | | Single nucleotide variant (intron variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +5 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (intron variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Age related macular degeneration 9 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (missense variant) | Age related macular degeneration 9 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Complement component 3 deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | C3-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Complement component 3 deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome with C3 anomaly +3 more | |
| | | Duplication (frameshift variant) | Complement component 3 deficiency +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Complement component 3 deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |