| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862187, RASGRF1 (E824K +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (G32S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (S771L +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (S733L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (K731N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (P731L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862187, RASGRF1 (P711A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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