| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CMTM6, LOC129936423 (M31T) | Single nucleotide variant (missense variant) | not specified | |
| | CMTM6, LOC129936423 (G32V) | Single nucleotide variant (missense variant) | not specified | |
| | CMTM6, LOC129936423 (T11M) | Single nucleotide variant (missense variant) | not specified | |
| | CMTM6, LOC129936423 (G16A) | Single nucleotide variant (missense variant) | not specified | |
| | CMTM6, LOC129936423 (R22Q) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
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