| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FPGT-TNNI3K, TNNI3K (F665L +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FPGT-TNNI3K, LRRC53
+1 more (E720fs +1 more) | Duplication (frameshift variant +1 more) | See cases +2 more | |
| | FPGT-TNNI3K, LRRC53
+1 more (N735K +2 more) | Single nucleotide variant (missense variant +1 more) | Atrial conduction disease | |
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