| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DIP2C, LOC126860805 (V1150I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DIP2C, LOC126860805 (D1138E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DIP2C, LOC126860805 (A1123P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DIP2C, LOC126860805 (T1107M) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | DIP2C, LOC126860805 (A1101V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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