| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126859847, SYNJ2 (R647G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859847, SYNJ2 (I646T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859847, SYNJ2 (R380H +1 more) | Single nucleotide variant (missense variant) | Meniere disease | |
| | LOC126859847, SYNJ2 (R617C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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