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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNI3
(R186W)
Single nucleotide variant
(missense variant)
SUDDEN INFANT DEATH SYNDROME
+4 more
GConflicting classifications of pathogenicity
TNNI3
(R145W)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+3 more
GPathogenic