| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | 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 | |
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