| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | FPGT-TNNI3K, TNNI3K (G526D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | FPGT-TNNI3K, TNNI3K (T539A +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | FPGT-TNNI3K, LRRC53
+1 more (E768K +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
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