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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1C
(R518C +1 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+3 more
GPathogenic
CACNA1C
(N537D +1 more)
Single nucleotide variant
(missense variant)
Timothy syndrome
+1 more
GLikely pathogenic
CACNA1C
(T1165A +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
GUncertain significance
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