| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IGF2, INS-IGF2 (C71R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GPathogenic/Likely risk allele |
Click to view in NCBI Gene