| | | Single nucleotide variant (intron variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Indel (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (intron variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant +1 more) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion | Heterotaxy, visceral, 1, X-linked +2 more | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Microsatellite (inframe_insertion) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant +1 more) | Heterotaxy, visceral, 1, X-linked +1 more | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked +1 more | GPathogenic/Likely pathogenic |
| | | Duplication | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (inframe_deletion) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (missense variant) | VACTERL association, X-linked, with or without hydrocephalus +2 more | |
| | | Single nucleotide variant (missense variant) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Heterotaxy, visceral, 1, X-linked +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | VACTERL association, X-linked, with or without hydrocephalus +1 more | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Microsatellite (inframe_deletion) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Microsatellite (inframe_deletion) | Heterotaxy, visceral, 1, X-linked | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (nonsense) | Heterotaxy, visceral, 1, X-linked | |
| | | Indel | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion (frameshift variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Congenital heart defects 1, nonsyndromic, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Congenital heart defects 1, nonsyndromic, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +2 more | |
| | | Deletion (3 prime UTR variant +1 more) | Congenital heart defects 1, nonsyndromic, 1 +2 more | |
| | | Deletion (3 prime UTR variant +1 more) | Congenital heart defects 1, nonsyndromic, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | VACTERL association, X-linked, with or without hydrocephalus +2 more | |
| | | Single nucleotide variant (intron variant +1 more) | Heterotaxy, visceral, 1, X-linked +2 more | |
| | | Single nucleotide variant (synonymous variant) | VACTERL association, X-linked, with or without hydrocephalus +2 more | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital heart defects 1, nonsyndromic, 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Microsatellite (inframe_insertion) | Heterotaxy, visceral, 1, X-linked +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Duplication | Heterotaxy, visceral, 1, X-linked | |
| | | Deletion | Heterotaxy, visceral, 1, X-linked | |
| | | Single nucleotide variant (synonymous variant) | Heterotaxy, visceral, 1, X-linked +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |