| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126805714, RIMS3 (G234S) | Single nucleotide variant (missense variant) | RIMS3-related condition | |
| | LOC126805714, RIMS3 (A207T) | Single nucleotide variant (missense variant) | RIMS3-related condition | |
| | | Single nucleotide variant (synonymous variant) | RIMS3-related condition | |
| | LOC126805714, RIMS3 (P185A) | Single nucleotide variant (missense variant) | RIMS3-related condition | |
| | | Single nucleotide variant (synonymous variant) | RIMS3-related condition | |
| | LOC126805714, RIMS3 (A163T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805714, RIMS3 (P220S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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