| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EPB41L2, LOC121740666 (H898Q +10 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EPB41L2, LOC121740666 (I807V +10 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EPB41L2, LOC121740666 (R695I +10 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EPB41L2, LOC121740666 (G476E +10 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EPB41L2, LOC121740666 (G967R +10 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene