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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLP1, RAB9B
Single nucleotide variant
(5 prime UTR variant)
Pelizaeus-Merzbacher disease
+2 more
GBenign/Likely benign
PLP1, RAB9B
Single nucleotide variant
(synonymous variant +1 more)
Hereditary spastic paraplegia 2
+4 more
GBenign/Likely benign