| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FRAS1, LOC126807089 (Q3650*) | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | FRAS1, LOC126807089 (R3654C) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
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