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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GBA1, LOC106627981
(D405V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GBA1, LOC106627981
(T408M +2 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
GBA1, LOC106627981
(E365K +2 more)
Single nucleotide variant
(missense variant)
not specified
+13 more
GBenign/Likely benign; risk factor
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