| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GCDH, LOC126862860 +1 more | Single nucleotide variant (synonymous variant +2 more) | Glutaric aciduria, type 1 +2 more | |
| | LOC126862860, SYCE2 (S197F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862860, SYCE2 (R184C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862860, SYCE2 (P182L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862860, SYCE2 (K180T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SYCE2, LOC126862860 (V153M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene