| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LDB1, LOC126861021 (E133D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LDB1, LOC126861021 (C159S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LDB1, LOC126861021 (V6M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LDB1, LOC126861021 (Q66P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LDB1, LOC126861021 (Q125H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene