| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130067398, SLC16A8 (T71M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | LOC130067398, SLC16A8 (L68F) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
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