| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | MIR3936HG, SLC22A4 (V172I) | Single nucleotide variant (missense variant) | not provided | |
| | LOC129994569, MIR3936HG
+1 more | Single nucleotide variant (5 prime UTR variant) | Renal carnitine transport defect +1 more | GConflicting classifications of pathogenicity |
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