| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (3 prime UTR variant) | IGF1-related condition | |
| | IGF1, LINC02456 (A118T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | IGF1-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | IGF1-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
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