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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT1
Single nucleotide variant
(intron variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
TNNT1
(E180* +1 more)
Single nucleotide variant
(nonsense)
Nemaline myopathy 5
GPathogenic