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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPEG
(R1055W)
Single nucleotide variant
(missense variant)
Myopathy, centronuclear, 5
GUncertain significance
SPEG
(R1234W)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
ASIC4-AS1, SPEG
(R2747C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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