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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF170
Single nucleotide variant
(synonymous variant)
Spastic paraplegia 85, autosomal recessive
GUncertain significance
RNF170
(R116* +1 more)
Single nucleotide variant
(nonsense)
Spastic paraplegia 85, autosomal recessive
+1 more
GConflicting classifications of pathogenicity
RNF170
(C102R +1 more)
Single nucleotide variant
(missense variant +1 more)
Spastic paraplegia 85, autosomal recessive
+1 more
GConflicting classifications of pathogenicity
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