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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYORG
Microsatellite
(inframe_deletion)
not provided
+1 more
GConflicting classifications of pathogenicity
MYORG
(G107R)
Single nucleotide variant
(missense variant)
Basal ganglia calcification, idiopathic, 7, autosomal recessive
GUncertain significance