| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +3 more | |
Click to view in NCBI Gene