| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene