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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCM2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GCM2
(T370M)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
GCM2
(A148T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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