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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PNPLA2
Single nucleotide variant
(synonymous variant)
Neutral lipid storage myopathy
GConflicting classifications of pathogenicity
PNPLA2
(E368Q)
Single nucleotide variant
(missense variant)
Neutral lipid storage myopathy
GUncertain significance
PNPLA2
Single nucleotide variant
(intron variant)
Neutral lipid storage myopathy
GUncertain significance
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