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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB9B, PLP1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+5 more
GBenign
PLP1, RAB9B
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign/Likely benign