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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1S
(R1086C)
Single nucleotide variant
(missense variant)
not specified
+5 more
GUncertain significance
GH-LCR, SCN4A
(R1740W)
Single nucleotide variant
(missense variant)
Hyperkalemic periodic paralysis
+5 more
GUncertain significance