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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SORD
(A153D)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
SORD
(A253fs)
Deletion
(frameshift variant +1 more)
Neuromuscular disease
+5 more
GPathogenic/Likely pathogenic