| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129992983, NEUROG2 (L201P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992983, NEUROG2 (A200V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992983, NEUROG2 (A197P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992983, NEUROG2 (G195A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992983, NEUROG2 (G177D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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