| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | IPCEF1, OPRM1 (S137L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IPCEF1, OPRM1 (T145S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IPCEF1, OPRM1 (I141L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IPCEF1, OPRM1 (I438V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IPCEF1, OPRM1 (V308G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Tramadol response | |
| | | Single nucleotide variant (intron variant) | Tramadol response | |
| | | Single nucleotide variant (intron variant) | Tramadol response | |
| | | Single nucleotide variant (synonymous variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (synonymous variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Tramadol response | |
| | | Single nucleotide variant (intron variant) | Tramadol response | |
| | IPCEF1, OPRM1 (S184P +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
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