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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126860498, WASHC5
(T1106M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WASHC5
(A1049T +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 8
+2 more
GUncertain significance
WASHC5, WASHC5-AS1
(R711H +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
+1 more
GUncertain significance
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