| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | LOC129993734, RETREG1 +1 more | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | LOC129993734, RETREG1 +1 more | Single nucleotide variant (5 prime UTR variant) | Neuropathy, hereditary sensory and autonomic, type 2B +1 more | |
Click to view in NCBI Gene