| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | C2orf69, LOC129935377 (L6P) | Single nucleotide variant (missense variant) | not provided | |
| | C2orf69, LOC129935377 (W2L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | C2orf69, LOC129935377 (S28C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene