| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FPGT-TNNI3K, LRRC53
+1 more | Single nucleotide variant (intron variant) | not provided | |
| | FPGT-TNNI3K, LRRC53
+1 more (P742L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
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