| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC122817729, SLC20A1 (I26V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC122817729, SLC20A1 (N96S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | SLC20A1-related disorder | |
| | LOC122817729, SLC20A1 (Q99E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC122817729, SLC20A1 (K87T) | Single nucleotide variant (missense variant) | not specified | |
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