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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C19orf12
(K131T +2 more)
Single nucleotide variant
(missense variant +1 more)
Neurodegeneration with brain iron accumulation 4
+4 more
GBenign
C19orf12
(T11M)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+3 more
GPathogenic/Likely pathogenic