| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | DYNLT2B-related disorder +1 more | |
| | LOC129938285, TM4SF19-DYNLT2B +1 more | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | DYNLT2B, LOC129938285 +1 more | Duplication (5 prime UTR variant) | DYNLT2B-related disorder | |
Click to view in NCBI Gene