| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FPGT-TNNI3K, TNNI3K (I686T +1 more) | Single nucleotide variant (missense variant) | TNNI3K-related condition +2 more | |
| | FPGT-TNNI3K, LRRC53
+1 more | Single nucleotide variant (intron variant) | not provided | |
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