| | FLNA, LOC107988032 (F2570L +1 more) | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 | |
| | | Single nucleotide variant (synonymous variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +9 more | |
| | FLNA, LOC107988032 (P2630L +1 more) | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | not specified +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Heterotopia, periventricular, X-linked dominant +9 more | |
| | | Single nucleotide variant (synonymous variant) | Melnick-Needles syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Terminal osseous dysplasia-pigmentary defects syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Terminal osseous dysplasia-pigmentary defects syndrome +11 more | |
| | | Duplication | Heterotopia, periventricular, X-linked dominant +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Heterotopia, periventricular, X-linked dominant +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiac valvular dysplasia, X-linked +10 more | |
| | | Single nucleotide variant (missense variant) | Melnick-Needles syndrome +10 more | |
| | TAFAZZIN, DNASE1L1 +3 more | Duplication | Frontometaphyseal dysplasia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability +4 more | |
| | | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 +3 more | |
| | | Duplication | Frontometaphyseal dysplasia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +10 more | |
| | | Single nucleotide variant (missense variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +8 more | |
| | | Single nucleotide variant (synonymous variant) | FLNA-related disorder +12 more | |
| | | Single nucleotide variant (missense variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia +6 more | GConflicting classifications of pathogenicity |
| | | Duplication | Frontometaphyseal dysplasia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Melnick-Needles syndrome +6 more | |
| | | Duplication | Melnick-Needles syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Familial thoracic aortic aneurysm and aortic dissection +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiac valvular dysplasia, X-linked +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | FG syndrome 2 +10 more | |
| | | Single nucleotide variant (intron variant) | FG syndrome 2 +10 more | |
| | | Single nucleotide variant (missense variant) | FG syndrome 2 +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | FG syndrome 2 +9 more | |
| | | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | FG syndrome 2 +11 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +12 more | |
| | FLNA, LOC107988032 (C2535Y +1 more) | Single nucleotide variant (missense variant) | not provided +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +13 more | |
| | | Single nucleotide variant (missense variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | FLNA-related disorder +14 more | |
| | | Single nucleotide variant (missense variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +12 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +12 more | |
| | | Single nucleotide variant (synonymous variant) | FLNA-related disorder +13 more | |
| | | Single nucleotide variant (intron variant) | Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked +10 more | |
| | | Single nucleotide variant (missense variant) | FLNA-related disorder +12 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Frontometaphyseal dysplasia +11 more | |
| | | Single nucleotide variant (intron variant) | Connective tissue disorder +12 more | |
| | | Single nucleotide variant (synonymous variant) | Heterotopia, periventricular, X-linked dominant +12 more | |
| | | Single nucleotide variant (synonymous variant) | Heterotopia, periventricular, X-linked dominant +13 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Oto-palato-digital syndrome, type II +13 more | |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +13 more | |
| | | Single nucleotide variant (missense variant) | Oto-palato-digital syndrome, type II +13 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Frontometaphyseal dysplasia 1 | |