| | ATIC, FN1 (S2131T +16 more) | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Indel (nonsense +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Glomerulopathy with fibronectin deposits 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Spondylometaphyseal dysplasia - Sutcliffe type +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder | |
| | | Indel (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder +1 more | |
| | FN1, LOC126806497 (R1392H +1 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (splice donor variant) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Deletion (intron variant) | Glomerulopathy with fibronectin deposits 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Spondylometaphyseal dysplasia - Sutcliffe type +3 more | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Spondylometaphyseal dysplasia - Sutcliffe type +3 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | FN1-related disorder +1 more | |