| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ACSM4, LOC126861434 (G231V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ACSM4, LOC126861434 (I248T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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