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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP2U1, CYP2U1-AS1
(P10Q)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GUncertain significance
CYP2U1, CYP2U1-AS1
(G35D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP2U1, CYP2U1-AS1
(V69A)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CYP2U1, CYP2U1-AS1
+1 more
(P151Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
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