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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GDI1
Single nucleotide variant
(intron variant)
GDI1-related condition
+3 more
GBenign
GDI1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
GDI1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
GDI1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
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