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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WASHC5
Single nucleotide variant
(intron variant)
Hereditary spastic paraplegia 8
+2 more
GUncertain significance
WASHC5
(R522Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 8
GUncertain significance
WASHC5
Single nucleotide variant
(splice donor variant)
Hereditary spastic paraplegia 8
GLikely pathogenic
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