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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNI3, TNNT1
(E12G)
Single nucleotide variant
(missense variant)
Nemaline myopathy 5
+5 more
GBenign/Likely benign
TNNT1, TNNI3
Single nucleotide variant
(5 prime UTR variant)
Dilated Cardiomyopathy, Recessive
+6 more
GBenign/Likely benign