| | | Single nucleotide variant (missense variant +1 more) | Holoprosencephaly 7 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PTCH1-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PTCH1-related disorder +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | PTCH1-related disorder +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | PTCH1-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Holoprosencephaly 7 +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | PTCH1-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Basal cell carcinoma, susceptibility to, 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Holoprosencephaly 7 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Holoprosencephaly 7 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Holoprosencephaly 7 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PTCH1-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Holoprosencephaly 7 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Anophthalmia-microphthalmia syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | Holoprosencephaly 7 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | PTCH1-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PTCH1-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | PTCH1-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Holoprosencephaly 7 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | PTCH1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PTCH1-related disorder +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gorlin syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | PTCH1-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |