| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC124418421, STIM1 (S437N +9 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Stormorken syndrome +3 more | |
| | LOC124418421, STIM1 (P605A +9 more) | Single nucleotide variant (missense variant +2 more) | not specified +3 more | |
| | LOC124418421, STIM1 (P466S +9 more) | Single nucleotide variant (missense variant +2 more) | STIM1-related condition | |
| | LOC124418421, STIM1 (R643H +9 more) | Single nucleotide variant (missense variant +2 more) | Stormorken syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +4 more | |
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