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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C19orf12
(G69R +1 more)
Single nucleotide variant
(missense variant +1 more)
Mental deterioration
+8 more
GPathogenic/Likely pathogenic
C19orf12
(G54E +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary spastic paraplegia 43
+2 more
GPathogenic/Likely pathogenic
C19orf12
(K8N)
Single nucleotide variant
(5 prime UTR variant +1 more)
Neurodegeneration with brain iron accumulation 4
GPathogenic
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