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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC110121288, SCN10A
(M1161T +2 more)
Single nucleotide variant
(missense variant)
Brugada syndrome
+4 more
GConflicting classifications of pathogenicity
LOC110121288, SCN10A
(I890F +1 more)
Single nucleotide variant
(missense variant)
Episodic pain syndrome, familial, 2
GUncertain significance