| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (intron variant) | STIM1-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | STIM1-related condition +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Myopathy, tubular aggregate, 1 +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | STIM1-related condition +3 more | |
| | | Duplication (intron variant) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (intron variant) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant) | STIM1-related condition | |
| | | Single nucleotide variant (intron variant) | STIM1-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | STIM1-related condition +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Combined immunodeficiency due to STIM1 deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | STIM1-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | STIM1-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | STIM1-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Indel (inframe_indel +1 more) | STIM1-related condition | |
| | | Single nucleotide variant (missense variant +2 more) | STIM1-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | Myopathy with tubular aggregates +3 more | |
| | LOC124418421, STIM1 (S437N +9 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +4 more | |
| | LOC124418421, STIM1 (P466S +9 more) | Single nucleotide variant (missense variant +2 more) | STIM1-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | STIM1-related condition +4 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | STIM1-related condition | |