| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC126806950, RGS12 (A149V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC126806950, RGS12 (P41L +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806950, RGS12 (G858S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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