| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GFRA4, LOC130065333 (L153P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GFRA4, LOC130065334 (S108L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GFRA4, LOC130065334 (P139Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GFRA4, LOC130065333 (R175G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene